Cas 133191-93-2,3-Chloro-benzoic acid (2R,3S,4R,5R)-3,4,5,6-tetraacetoxy-tetrahydro-pyran-2-yl ester

133191-93-2

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Basic information

Product Name: 3-Chloro-benzoic acid (2R,3S,4R,5R)-3,4,5,6-tetraacetoxy-tetrahydro-pyran-2-yl ester
Synonyms: 3-Chloro-benzoic acid (2R,3S,4R,5R)-3,4,5,6-tetraacetoxy-tetrahydro-pyran-2-yl ester
CAS NO:133191-93-2
Molecular Formula:
Molecular Weight: 472.833
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: 3-Chloro-benzoic acid (2R,3S,4R,5R)-3,4,5,6-tetraacetoxy-tetrahydro-pyran-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Chloro-benzoic acid (2R,3S,4R,5R)-3,4,5,6-tetraacetoxy-tetrahydro-pyran-2-yl ester(133191-93-2)
EPA Substance Registry System: 3-Chloro-benzoic acid (2R,3S,4R,5R)-3,4,5,6-tetraacetoxy-tetrahydro-pyran-2-yl ester(133191-93-2)

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: 133191-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133191-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,1,9 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133191-93:
(8*1)+(7*3)+(6*3)+(5*1)+(4*9)+(3*1)+(2*9)+(1*3)=112
112 % 10 = 2
So 133191-93-2 is a valid CAS Registry Number.

133191-93-2Upstream product

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133191-93-2Relevant academic research and scientific papers

Conversion of D-Glucose to L-Glucose: Oxidative Decarboxylation of α-Oxy Carboxylic Acids via Their Diacyl Peroxides

Shiozaki, Masao

, p. 528 - 532 (2007/10/02)

D-Glucose was converted to an L-glucose derivative.The key step was the oxidative decarboxylation of carboxylic acid 12 via its diacyl peroxide derivative.This synthetic scheme proceeds through C-glycosidic compounds and is applicable to other sugar confi

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