353764-08-6

Basic information

• Product Name: (S)-2-[(2-iodobenzoyl)amino]-3-methyl-1-butanol
• Synonyms: (S)-2-[(2-iodobenzoyl)amino]-3-methyl-1-butanol
• CAS NO: 353764-08-6
• Molecular Weight: 333.169
• Mol File: 353764-08-6.mol

Chemical Properties

• CAS DataBase Reference: (S)-2-[(2-iodobenzoyl)amino]-3-methyl-1-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-[(2-iodobenzoyl)amino]-3-methyl-1-butanol(353764-08-6)
• EPA Substance Registry System: (S)-2-[(2-iodobenzoyl)amino]-3-methyl-1-butanol(353764-08-6)

Safety Data

• Hazardous Substances Data: 353764-08-6(Hazardous Substances Data)

Upstream product

• 294665-21-7 (S)-methyl 2-[(2-iodobenzoyl)amino]-3-methylbutanoate 
• 609-67-6 2-Iodobenzoyl chloride 
• 6306-52-1 L-valine methylester hydrochloride 
• 2026-48-4 (S)-valinol 

Downstream Products

• 694458-98-5 2-(2-iodophenyl)-4-isopropyl-4,5-dihydrooxazole 
• 353764-11-1 (S,E)-methyl 4-[(2-iodobenzoyl)amino]-5-methyl-2-hexenoate 

Relevant articles and documents

Asymmetric oxidation of o-alkylphenols with chiral 2-(o-lodoxyphenyl)- oxazolines

A new class of chiral iodine(V) derivatives has been prepared. These compounds have been found to transform ortho-alkylphenols into ortho-quinol Diels-Alder dimers with significant levels of asymmetric induction.

Efficient Synthesis of Chiral Isoquinoline and Pyrido[1,2-b]-isoquinoline Derivatives via Intramolecular Heck Reactions

The palladium(0)-catalyzed reaction of derivatives of γ-amino-α,β-unsaturated esters bearing an N-(2-iodobenzoyl) substituent results in an intramolecular Heck reaction, the outcome of which depends on the structure of the substrate as well as on the expe