154458-49-8

Basic information

• Product Name: [4-(tert-Butyl-diphenyl-silanyloxy)-phenyl]-acetaldehyde
• CAS NO: 154458-49-8
• Molecular Weight: 374.555
• Mol File: 154458-49-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [4-(tert-Butyl-diphenyl-silanyloxy)-phenyl]-acetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(tert-Butyl-diphenyl-silanyloxy)-phenyl]-acetaldehyde(154458-49-8)
• EPA Substance Registry System: [4-(tert-Butyl-diphenyl-silanyloxy)-phenyl]-acetaldehyde(154458-49-8)

Safety Data

• Hazardous Substances Data: 154458-49-8(Hazardous Substances Data)

Upstream product

• 501-94-0 p-hydroxyphenethyl alcohol 
• 7339-87-9 4-hydroxyphenylacetaldehyde 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 154458-48-7 (2S,3R)-1-[4-(tert-Butyl-diphenyl-silanyloxy)-phenyl]-4-(1H-indol-3-yl)-butane-2,3-diol 
• 154458-46-5 1-[4-(tert-Butyl-diphenyl-silanyloxy)-phenyl]-but-3-en-2-ol 

Relevant articles and documents

ASYMMETRIC SYNTHESIS OF THE ANTICOCCIDIAL ANTIBIOTIC DIOLMYCIN A1. DETERMINATION OF ABSOLUTE STEREOCHEMISTRY

An asymmetric total synthesis of diolmycin A1 (1), a recently discovered anticoccidial antibiotic, has been achieved in six steps from 2-(4-hydroxyphenyl)ethanol.The natural product comprises an unusual ca. 4:1 mixture of enantiomers; the synthesis defined the (11R,12S) absolute configuration of the predominant (-) antipode.