97055-79-3

Basic information

• Product Name: 4-Benzyloxy-2-methylbutanal
• Synonyms: 4-Benzyloxy-2-methylbutanal
• CAS NO: 97055-79-3
• Molecular Weight: 192.258
• Mol File: 97055-79-3.mol

Chemical Properties

• CAS DataBase Reference: 4-Benzyloxy-2-methylbutanal(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Benzyloxy-2-methylbutanal(97055-79-3)
• EPA Substance Registry System: 4-Benzyloxy-2-methylbutanal(97055-79-3)

Safety Data

• Hazardous Substances Data: 97055-79-3(Hazardous Substances Data)

Upstream product

• 71312-15-7 3-((benzyloxy)methyl)-2,2-dimethyloxirane 
• 6278-91-7 4-(benzyloxy)-2-butanone 
• 75-16-1 methylmagnesium bromide 
• 89956-14-9 [3-(2-Benzyloxyethyl)oxiran-2-yl]methanol 

Downstream Products

• 944994-45-0 C₂₃H₃₈O₄ 
• 96154-47-1 (R)-2-methyl-1,4-butanediol 4-benzyl ether 
• 944994-42-7 C₃₄H₄₆Br₂O₆ 
• 944994-50-7 C₃₄H₄₈Br₂O₆ 
• 944994-48-3 C₃₄H₅₄O₄ 
• 944994-46-1 C₂₁H₃₄O₃ 
• 96154-46-0 (R,S)-2-methyl-4-(phenylmethyloxy)butan-1-ol 
• 66261-30-1 (S)-4-(benzyloxy)-2-methylbutan-1-ol 
• 80325-81-1 (2S,3S)-5-Benzyloxy-3-methyl-pentan-2-ol 
• 80325-81-1 (2R,3S)-5-Benzyloxy-3-methyl-pentan-2-ol 

Relevant articles and documents

A total synthesis of the unique tris-oxazole macrolide ulapualide a produced by the marine nudibranch Hexabranchus sanguineus

A total synthesis of ulapualide A (1), whose relative stereochemistry was assigned on the basis of an earlier molecular mechanics study of its hypothetical metal chelated complex 9, is described. The synthesis is based on: i, elaboration of the double fun

Studies on the enantioselectivity of the transesterification of 2-methyl-1,4-butanediol and its derivatives catalyzed by Pseudomonas fluorescens lipase in organic solvents

The irreversible transesterification of 2-methy-1,4-butanediol 1a and its benzyl ethers 2a and 3a catalyzed by Pseudomonas fluorescens lipase in chloroform was studied, the highest ee (> 98%) having been obtained for the 4-benzyl ether 2a.