Cas 187930-97-8,(S)-1-{(2R,5S)-5-[(R)-2-(2,6-Dichloro-benzyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-yl}-propan-2-ol

187930-97-8

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Basic information

Product Name: (S)-1-{(2R,5S)-5-[(R)-2-(2,6-Dichloro-benzyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-yl}-propan-2-ol
Synonyms:
CAS NO:187930-97-8
Molecular Formula:
Molecular Weight: 347.282
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-1-{(2R,5S)-5-[(R)-2-(2,6-Dichloro-benzyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-yl}-propan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-{(2R,5S)-5-[(R)-2-(2,6-Dichloro-benzyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-yl}-propan-2-ol(187930-97-8)
EPA Substance Registry System: (S)-1-{(2R,5S)-5-[(R)-2-(2,6-Dichloro-benzyloxy)-1-methyl-ethyl]-tetrahydro-furan-2-yl}-propan-2-ol(187930-97-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 187930-97-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 187930-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,9,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 187930-97:
(8*1)+(7*8)+(6*7)+(5*9)+(4*3)+(3*0)+(2*9)+(1*7)=188
188 % 10 = 8
So 187930-97-8 is a valid CAS Registry Number.

187930-97-8Upstream product

20443-98-5 2,6-Dichlorobenzyl bromide

187930-97-8Downstream Products

187930-97-8Relevant academic research and scientific papers

An Enantioselective Synthesis of (-)-Nonactic Acid and (+)-8-epi-Nonactic Acid Using Microbial Reduction

Takatori, Kazuhiko,Tanaka, Kenji,Matsuoka, Katsunori,Morishita, Kazuyoshi,Kajiwara, Masahiro

, p. 159 - 160 (1997)

An enantioselective synthesis of (-)-nonactic acid (2a) and (+)-8-epi-nonactic acid (2b) is described. The microbial reduction of the dl-ketone 3 with baker's yeast gave two easily separable diastereomeric alcohols 11a and 11b, each in over 97% ee. These alcohols were converted to 2a and 2b in 4 steps.

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