75420-45-0

Basic information

• Product Name: (S)-(+)-3-methyl-4-penten-1-ol
• CAS NO: 75420-45-0
• Molecular Weight: 100.161
• Mol File: 75420-45-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (S)-(+)-3-methyl-4-penten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-3-methyl-4-penten-1-ol(75420-45-0)
• EPA Substance Registry System: (S)-(+)-3-methyl-4-penten-1-ol(75420-45-0)

Safety Data

• Hazardous Substances Data: 75420-45-0(Hazardous Substances Data)

Upstream product

• 75371-84-5 (S)-(+)-3-methyl-4-pentenoic acid 
• 20459-97-6 3-Methyl-4-pentensaeure-methylester 
• 40930-20-9 (2Z)-3-methylpenta-2,4-dien-1-ol 
• 54716-03-9 3-methylpenta-2(Z),4-dien-1-al 
• 6153-06-6 (E)-3-methylpent-2-en-4-yn-1-ol 
• 6153-05-5 (Z)-3-methylpent-2-en-4-ynol 
• 2436-90-0 (S)-(+)-dihydromyrcene 
• 80654-41-7 (R)-3-methyl-5-o-nitrophenylselenopentanoic acid 
• 67-56-1 methanol 
• 64234-27-1 ((1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-yl)borane 
• 220131-44-2 1,1,4-trimethyl-1,2,3,6-tetrahydro-siline 
• 19776-07-9 S-(+)-2,6-dimethyl-7-octen-3-one 
• 75371-83-4 (S)-(+)-3-methyl-4-pentenyl acetate 
• 1572-08-3 (E)-3-methylpenta-2,4-dien-1-ol 

Downstream Products

• 22460-59-9 (3R/S,6S)-2,6-dimethyl-1,7-octadien-3-ol 
• 54702-01-1 (S)-2,6,6-Trimethyl-1-(3-methyl-pent-4-enyl)-cyclohexa-2,4-dienol 

Relevant articles and documents

A ring-closing metathesis approach to cyclic α,β-dehydroamino acids

A comprehensive study on the synthesis and ring-closing metathesis (RCM) of α,β-dehydroamino acids is described. This sequence has led to the formation of a range of biologically relevant functionalized nitrogen heterocycles. The incorporation of chiral b

REGIO- AND STEREOSELECTIVE HYDROGENATION OF METHYL SUBSTITUTED PENTADIEN-1-OLS BY BAKER'S YEAST

(E)-2-methyl and (E)-3-methyl-2,4-pentadien-1-ols are reduced to (S)-2-methyl- and (S)-3-methyl-4-penten-1-ols, respectively, using baker's yeast as a regio- and stereoselective reagent.This microbiological conversion provides an efficient route to bifunctional and enantiomerically pure C6-building blocks containing the C'-CH(Me)-C'' grouping.

Stereoselective Synthesis of (S,E)-6-Isopropyl-3,9-dimethyl-5,8-decadienyl Acetate, the (S)-Enantiomer of the Yellow Scale Pheromone

The (S)-enantiomer of the sex pheromone of the yellow scale (Aonidiella citrina), (S,E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, was stereoselectively synthesized from (R)-(+)-citronellic acid.