95338-10-6

Basic information

• Product Name: 3-Pentanol, 1-(phenylmethoxy)-, (R)-
• CAS NO: 95338-10-6
• Molecular Formula: C12H18O2
• Molecular Weight: 194.274
• Mol File: 95338-10-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Pentanol, 1-(phenylmethoxy)-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pentanol, 1-(phenylmethoxy)-, (R)-(95338-10-6)
• EPA Substance Registry System: 3-Pentanol, 1-(phenylmethoxy)-, (R)-(95338-10-6)

Safety Data

• Hazardous Substances Data: 95338-10-6(Hazardous Substances Data)

Upstream product

• 95338-09-3 (R)-1,3-pentanediol 1-benzyl, 3-(2-tetrahydropyranyl) ether 
• 96120-11-5 methyl (R)-3-tetrahydropyranyloxypentanoate 
• 95337-99-8 (R)-1,3-pentanediol 1-t-butyldimethylsilyl, 3-(2-tetrahydropyranyl) ether 
• 95337-98-7 (R)-1,3-pentanediol 1-t-butyldimethylsilyl ether 
• 95338-00-4 (R)-1,3-pentanediol 3-(2-tetrahydropyranyl) ether 
• 42558-50-9 methyl (3R)-3-hydroxypentanoate 
• 19790-60-4 3-Benzyloxypropanal 
• 557-20-0 diethylzinc 
• 95338-08-2 methyl (3R)-3-(3',5'-dinitrobenzoyloxy)-pentanoate 

Downstream Products

• 95338-12-8 (S)-1,3-pentanediol 1-benzyl ether 
• 89672-11-7 cyoctol 
• 89672-11-7 cyoctol 
• 89672-11-7 cyoctol 
• 793685-17-3 C₂₃H₃₂SO₄C₅H₁₀O 
• 95338-01-5 (S)-1,3-pentanediol 3-(2-tetrahydropyranyl) ether 1-tosylate 

Relevant articles and documents

Stereocontrolled synthesis of all eight stereoisomers of the putative anti-androgen cyoctol

All eight stereoisomers (1-4 and enantiomers) of the putative anti-androgen cyoctol have been synthesized along stereochemically unambiguous routes. The biological tests of all isomers indicated that cyoctol is not an anti-androgen, contrary to the patent literature. All eight stereoisomers of the putative anti-androgen cyoctol have been prepared and tested biologically.

SYNTHESIS OF ALL OF THE FOUR ENERGETICALLY POSSIBLE STEREOISOMERS OF 7-ETHYL-2-METHYL-1,6-DIOXASPIRODECANE; A PHEROMONE PRODUCED BY BEES PARAVESPURA VULGARIS L. AND ANDRENA HAEMORRHOA F.

All of the four energetically possible stereoisomers of 7-ethyl-2-methyl-1,6-dioxaspirodecane were synthesized starting from ethyl (S)-lactate and dimethyl (S)-malate or methyl (R)-β-hydroxy-valerate employing dianion alkylation as the key-step.