Cas 191795-31-0,(3S,4S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-3,4-dihydroxy-cyclohex-1-enecarboxylic acid tert-butyl ester

191795-31-0

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Basic information

Product Name: (3S,4S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-3,4-dihydroxy-cyclohex-1-enecarboxylic acid tert-butyl ester
Synonyms: (3S,4S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-3,4-dihydroxy-cyclohex-1-enecarboxylic acid tert-butyl ester
CAS NO:191795-31-0
Molecular Formula:
Molecular Weight: 344.524
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: (3S,4S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-3,4-dihydroxy-cyclohex-1-enecarboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-3,4-dihydroxy-cyclohex-1-enecarboxylic acid tert-butyl ester(191795-31-0)
EPA Substance Registry System: (3S,4S,5S)-5-(tert-Butyl-dimethyl-silanyloxy)-3,4-dihydroxy-cyclohex-1-enecarboxylic acid tert-butyl ester(191795-31-0)

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: 191795-31-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 191795-31-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,7,9 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 191795-31:
(8*1)+(7*9)+(6*1)+(5*7)+(4*9)+(3*5)+(2*3)+(1*1)=170
170 % 10 = 0
So 191795-31-0 is a valid CAS Registry Number.

191795-31-0Upstream product

191795-31-0Downstream Products

10191-00-1 (+)-shikimic acid

191795-31-0Relevant academic research and scientific papers

Enantioselective synthesis of (+)-shikimic acid and (+)-5-epi-shikimic acid by asymmetric Diels-Alder reaction of (S)-α-sulfinylacrylates

Adrio, Javier,Carretero, Juan C.,Ruano, Jose L. Garcia,Cabrejas, Luisa M. Martin

, p. 1623 - 1631 (2007/10/03)

Enantiopure (S) benzyl and t-butyl 2-p-tolylsulfinylpropenoates (1 and 2) were readily prepared by Mannich condensation of (R) p-tolylsulfinylacetates (CH2O+Me2N'H), followed by in situ nitrogen quaternization. These new chiral dieno

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