Amerigo Scientific

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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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(Isopropenyloxy)trimethylsilane Inquiry  | >85%

Amerigo Scientific

(Isopropenyloxy)trimethylsilane is an enol silyl ether. It participates as nucleophile in Lewis acid-promoted C3-nucleophile substitution of tetracyclic bromide. It is reported to participate in the total synthesis of (±)-powelline. It is reported to participate in dityltin bis(triflate) catalyzed Michael addition reaction of enol silyl ethers.

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(Methyldiphenylsilyl)acetylene Inquiry  | Purity Not Available

Amerigo Scientific

(Methyldiphenylsilyl)acetylene is an organic building block. Various physical properties (boiling point and density) of (methyldiphenylsilyl)acetylene have been reported.

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(Methylthio)acetic acid Inquiry  | >99%

Amerigo Scientific

Formation of complexes of methyl thioacetate and copper(II) has been investigated. (Methylthio)acetic acid is an irreversible inhibitor of sarcosine oxidase and is effective in preventing the complete enzyme inactivation during modification.

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(Phenylsulfonyl)acetonitrile Inquiry  | >98%

Amerigo Scientific

Condensation reaction of (phenylsulfonyl)acetonitrile with benzaldehyde in water in heterogeneous phase in the presence and absence of anionic and cationic surfactants has been studied. Dehydrative alkylation of alcohols with (phenylsulfonyl)acetonitrile under modified Mitsunobu conditions has been investigated.

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(Phenylthio)acetyl chloride Inquiry  | Purity Not Available

Amerigo Scientific

(Phenylthio)acetyl chloride is an acid halide. It participates in the Friedel -Crafts acylation of arenes to afford α-sulfenylated acetophenones.

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(R,R)-(?)-N,N′-Dimethyl-1,2-cyclohexanediamine Inquiry  | >97%

Amerigo Scientific

(R,R)-(-)-N,N′-Dimethyl-1,2-cyclohexanediamine is a N,N′-dimethylated derivative of enantiopure 1,2-diaminocyclohexane. It can be formed during the hydrolysis of (R3a,R7a)-1,3-(dimethyl)-2-phenyl-2,3,3a,4,5,6,7,7a-octahydro-1H-1,3,2-benzodiazaphosphole 2-oxide using HCl-methanol.

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