Amerigo Scientific

With years of experience in the life sciences, Amerigo Scientific has integrated global cutting-edge technology resources to provide the latest technological equipment, instruments, biological products, and custom services for research institutions and enterprises in the biological, chemical, pharmaceutical, medical, and other industries.

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2,7,8-Trimethyl-3-quinolinecarboxylic acid ethyl ester Inquiry  | Purity Not Available

Amerigo Scientific

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2,7,8-Trimethyl-3-quinolinecarboxylic acid ethyl ester

2,7,8-Trimethylquinoline-3-carboxylic acid Inquiry  | Purity Not Available

Amerigo Scientific

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2,7,8-Trimethylquinoline-3-carboxylic acid

2,8-Bis(trifluoromethyl)-2′-(2-pyridyl)-4-quinolineacetonitrile Inquiry  | Purity Not Available

Amerigo Scientific

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2,8-Bis(trifluoromethyl)-2′-(2-pyridyl)-4-quinolineacetonitrile

2,8-Bis(trifluoromethyl)-4-quinolyl(1-oxypyrid-2-yl) methane Inquiry  | Purity Not Available

Amerigo Scientific

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2,8-Bis(trifluoromethyl)-4-quinolyl(1-oxypyrid-2-yl) methane

2,8-Dibromo-6,12-dihydro-6,6,12,12-tetrakis(4-octylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene Inquiry  | >98%

Amerigo Scientific

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2,8-Dibromo-6,12-dihydro-6,6,12,12-tetrakis(4-octylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene

2,8-Dichloropyrimido[5,4-d]pyrimidine Inquiry  | >95%

Amerigo Scientific

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2,8-Dichloropyrimido[5,4-d]pyrimidine

2,8-Dichloroquinoline Inquiry  | >96%

Amerigo Scientific

2,8-Dichloroquinoline can be synthesized from the reaction between 8-chloroquinoline-N-oxide and phosphoryl trichloride.

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2,8-Dichloroquinoline

2,8-Dimethyl-4-hydroxyquinoline Inquiry  | Purity Not Available

Amerigo Scientific

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2,8-Dimethyl-4-hydroxyquinoline

2,8-Dimethylquinoline-3-carboxylic acid ethyl ester Inquiry  | Purity Not Available

Amerigo Scientific

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2,8-Dimethylquinoline-3-carboxylic acid ethyl ester

2,8-Quinolinediol Inquiry  | Purity Not Available

Amerigo Scientific

2,8-Quinolinediol is a quinolone derivative. It has been reported as metabolite of 8-hydroxyquinoline-N-oxide in rabbits. Synthesis of 2,8-quinolinediol has been reported. It is reported as one of the six possible forms of 8-hydroxycarbostyril. It has been detected as new UV-absorbing compound (UAC) in cow milk and its structure was elucidated using HRMS and by 1H, […]

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2,8-Quinolinediol

2,9-Diazaspiro[5.5]undecan-3-one dihydrochloride Inquiry  | Purity Not Available

Amerigo Scientific

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2,9-Diazaspiro[5.5]undecan-3-one dihydrochloride

2′-Aminoacetanilide Inquiry  | >95%

Amerigo Scientific

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2′-Aminoacetanilide

2′-Chloro-4′-(4-chlorophenoxy)acetophenone Inquiry  | >95%

Amerigo Scientific

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2′-Chloro-4′-(4-chlorophenoxy)acetophenone

2′-Fluoroacetanilide Inquiry  | >95%

Amerigo Scientific

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2′-Fluoroacetanilide

2′-Hydroxy-5′-nitroacetophenone Inquiry  | >95%

Amerigo Scientific

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2′-Hydroxy-5′-nitroacetophenone

2′-Mercaptoacetophenone Inquiry  | >95%

Amerigo Scientific

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2′-Mercaptoacetophenone

2′-Nitro-4′-(trifluoromethyl)acetanilide Inquiry  | >95%

Amerigo Scientific

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2′-Nitro-4′-(trifluoromethyl)acetanilide

2′-Nitrobenzanilide Inquiry  | >95%

Amerigo Scientific

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2′-Nitrobenzanilide

2′-Oxo-1′,2′-dihydrospiro[cyclobutane-1,3′-indole]-5′-sulfonyl chloride Inquiry  | >95%

Amerigo Scientific

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2′-Oxo-1′,2′-dihydrospiro[cyclobutane-1,3′-indole]-5′-sulfonyl chloride

2′,3′-Difluoroacetophenone Inquiry  | >95%

Amerigo Scientific

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2′,3′-Difluoroacetophenone

2′,3′-Dimethyl-6′-nitroacetanilide Inquiry  | >95%

Amerigo Scientific

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2′,3′-Dimethyl-6′-nitroacetanilide

2′,4′-Dimethoxybiphenyl-4-carbaldehyde Inquiry  | >37%

Amerigo Scientific

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2′,4′-Dimethoxybiphenyl-4-carbaldehyde

2′,4′-Dimethylacetophenone Inquiry  | >95%

Amerigo Scientific

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2′,4′-Dimethylacetophenone

2′,6′-Dichlorobenzanilide Inquiry  | >95%

Amerigo Scientific

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2′,6′-Dichlorobenzanilide

2′,6′-Difluoroacetophenone Inquiry  | >95%

Amerigo Scientific

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2′,6′-Difluoroacetophenone

2(3)-(Tetrahydrofurfuryloxy)tetrahydropyran Inquiry  | >98%

Amerigo Scientific

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2(3)-(Tetrahydrofurfuryloxy)tetrahydropyran

2(5H)-Furanone Inquiry  | >98%

Amerigo Scientific

Chiral urea compounds catalyzed hetero-Michael addition reaction of 2(5H)-furanone (γ-crotonolactone) to pyrrolidine. The quorum sensing inhibition activity by 2(5H)-furanone was studied using bioindicator strains.

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2(5H)-Furanone

2(5H)-Thiophenone Inquiry  | Purity Not Available

Amerigo Scientific

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2(5H)-Thiophenone

2′-(Trifluoromethyl)acetophenone Inquiry  | >99%

Amerigo Scientific

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2′-(Trifluoromethyl)acetophenone

2′-(Trifluoromethyl)propiophenone Inquiry  | Purity Not Available

Amerigo Scientific

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2′-(Trifluoromethyl)propiophenone

2′-Aminoacetanilide Inquiry  | >98%

Amerigo Scientific

2′-Aminoacetanilide (2-aminoacetanilide, o-aminoacetanilide) can be prepared by the catalytic hydrogenation of 2-nitroacetanilide using 10%Pd/C (palladium/carbon).

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2′-Aminoacetanilide

2′-Aminoacetophenone Inquiry  | >98%

Amerigo Scientific

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2′-Aminoacetophenone

2′-Aminoacetophenone hydrochloride Inquiry  | Purity Not Available

Amerigo Scientific

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2′-Aminoacetophenone hydrochloride

2′-Benzoyl-2,4′-dichloroacetanilide Inquiry  | Purity Not Available

Amerigo Scientific

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2′-Benzoyl-2,4′-dichloroacetanilide

2′-Bromo-2,2,2-trifluoroacetophenone Inquiry  | >97%

Amerigo Scientific

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2′-Bromo-2,2,2-trifluoroacetophenone

2′-Bromo-2,6-dimethoxybiphenyl Inquiry  | >97%

Amerigo Scientific

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2′-Bromo-2,6-dimethoxybiphenyl

2′-Bromoacetophenone Inquiry  | >99%

Amerigo Scientific

2′-Bromoacetophenone (2-Bromoacetophenone) undergoes enantioselective addition reaction with phenylacetylene catalyzed by chiral camphorsulfonamide. It reacts with aliphatic primary amines in the presence of palladium catalyst to afford 3-methyleneisoindolin-1-ones.

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2′-Bromoacetophenone

2′-Bromoacetophenone dimethyl ketal Inquiry  | >95%

Amerigo Scientific

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2′-Bromoacetophenone dimethyl ketal

2′-Chloro-5′-(trifluoromethyl)acetophenone Inquiry  | Purity Not Available

Amerigo Scientific

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2′-Chloro-5′-(trifluoromethyl)acetophenone

2′-Chloroacetophenone Inquiry  | >97%

Amerigo Scientific

2′-Chloroacetophenone undergoes stereoselective reduction to (R)-2′-chloro-1-phenyl-ethanol by Saccharomyces cerevisiae B5. It is commonly used as lacrimator.

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2′-Chloroacetophenone

2′-Chlorodiphenyl-2,3,4,5,6-d5 Inquiry  | Purity Not Available

Amerigo Scientific

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2′-Chlorodiphenyl-2,3,4,5,6-d5

2′-Ethyl Simvastatin Inquiry  | >99%

Amerigo Scientific

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2′-Ethyl Simvastatin

2′-Fluoro-4′-methoxyacetophenone Inquiry  | >99%

Amerigo Scientific

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2′-Fluoro-4′-methoxyacetophenone

2′-Fluoro-6′-(trifluoromethyl)acetophenone Inquiry  | >98%

Amerigo Scientific

2′-Fluoro-6′-(trifluoromethyl)acetophenone is an aryl fluorinated building block.

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2′-Fluoro-6′-(trifluoromethyl)acetophenone

2′-Fluoroacetophenone Inquiry  | >97%

Amerigo Scientific

The enantioselective reduction of 2′-fluoroacetophenone has been investigated.

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2′-Fluoroacetophenone

2′-Fluorobiphenyl-3-carboxylic acid Inquiry  | Purity Not Available

Amerigo Scientific

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2′-Fluorobiphenyl-3-carboxylic acid

2′-formyl-biphenyl-3-carbonitrile Inquiry  | Purity Not Available

Amerigo Scientific

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2′-formyl-biphenyl-3-carbonitrile

2′-Formyl[1,1′-biphenyl]-2-carboxylic acid Inquiry  | Purity Not Available

Amerigo Scientific

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2′-Formyl[1,1′-biphenyl]-2-carboxylic acid

2′-Hydroxy-1′-acetonaphthone Inquiry  | >99%

Amerigo Scientific

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2′-Hydroxy-1′-acetonaphthone

2′-Hydroxy-3-phenylpropiophenone Inquiry  | >97%

Amerigo Scientific

2′-Hydroxy-3-phenylpropiophenone is a colorless to yellow liquid or solid. 2′-Hydroxy-3-phenylpropiophenone derivatives show antiarrhythmic,spasmolytic and local anaesthetic activities.

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2′-Hydroxy-3-phenylpropiophenone