76741-12-3

Basic information

• Product Name: (2S,3R)-3-methylhexane-1,2-diol
• Synonyms: (2S,3R)-3-methylhexane-1,2-diol
• CAS NO: 76741-12-3
• Molecular Weight: 132.203
• Mol File: 76741-12-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2S,3R)-3-methylhexane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R)-3-methylhexane-1,2-diol(76741-12-3)
• EPA Substance Registry System: (2S,3R)-3-methylhexane-1,2-diol(76741-12-3)

Safety Data

• Hazardous Substances Data: 76741-12-3(Hazardous Substances Data)

Upstream product

• 123-15-9 2-methylvaleraldehyde 
• 28116-85-0 (2S,3R)-threo-2-amino-3-methylhexanoic acid 
• 60182-96-9 2-amino-3-methylhexanoic acid 
• 76713-39-8 (2R,3R)-2-hydroxy-3-methylhexanoic acid 
• 75-24-1 trimethylaluminum 
• 94992-76-4 (2S,3R)-2,3-epoxy-1-hexanol 
• 111003-36-2 ((2R,3S)-3-propyloxiran-2-yl)methanol 
• 15681-48-8 lithium dimethylcuprate 
• 89395-00-6 2,3-epoxyhexan-1-ol 
• 63707-80-2 2-((E)-3-methyl-hex-2-enyloxy)-tetrahydro-pyran 
• 63707-80-2 2-((Z)-3-methyl-hex-2-enyloxy)-tetrahydro-pyran 
• 28112-76-7 (+/-)-threo-2-acetamino-3-methylhexanoic acid 
• 110918-65-5 (2'R,3'S)-2',3'-epoxyhexyl 3,5-dinitrobenzoate 
• 110918-65-5 (2'S,3'R)-2',3'-epoxyhexyl 3,5-dinitrobenzoate 

Downstream Products

• 110918-75-7 (2S,3S,4R)-2,4-dimethyl-3-tetrahydropyranyloxyheptyl tosylate 
• 72522-80-6 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R)-1-ethyl-2-methyl-pentyl ester 
• 110918-68-8 (2S,3R)-3-methyl-1-tosyloxy-2-hexanol 

Relevant articles and documents

The C2 selective nucleophilic substitution reactions of 2,3-epoxy alcohols mediated by trialkyl borates: The first endo-mode epoxide-opening reaction through an intramolecular metal chelate

(Matrix presented) Highly efficient C2 selective substitution reactions of 2,3-epoxy alcohols with nucleophiles were developed by using NaN 3-(CH3O)3B, NaSPh-(CH3O) 3B, or NaCN-(C2H5/

SYNTHESIS OF BOTH THE ENANTIOMERS OF INVICTOLIDE, A PHEROMONE COMPONENT OF THE RED IMPORTED FIRE ANT

Both the enantiomers of invictolide were synthesized in 17 steps from propargyl alcohol.

Absolute configuration of (-) 4 methylheptan 3 ol, a pheromone of the smaller European elm bark beetle, as determined by the synthesis of its (3R,4R) (+) and (3S,4R) (+) isomers

-