Cas 64790-65-4,Benzoic acid (1S,2R,3S,6R)-2,3-dihydroxy-7-oxa-bicyclo[4.1.0]hept-4-en-1-ylmethyl ester

64790-65-4

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Basic information

Product Name: Benzoic acid (1S,2R,3S,6R)-2,3-dihydroxy-7-oxa-bicyclo[4.1.0]hept-4-en-1-ylmethyl ester
Synonyms: Benzoic acid (1S,2R,3S,6R)-2,3-dihydroxy-7-oxa-bicyclo[4.1.0]hept-4-en-1-ylmethyl ester
CAS NO:64790-65-4
Molecular Formula:
Molecular Weight: 262.262
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: Benzoic acid (1S,2R,3S,6R)-2,3-dihydroxy-7-oxa-bicyclo[4.1.0]hept-4-en-1-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (1S,2R,3S,6R)-2,3-dihydroxy-7-oxa-bicyclo[4.1.0]hept-4-en-1-ylmethyl ester(64790-65-4)
EPA Substance Registry System: Benzoic acid (1S,2R,3S,6R)-2,3-dihydroxy-7-oxa-bicyclo[4.1.0]hept-4-en-1-ylmethyl ester(64790-65-4)

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: 64790-65-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 64790-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,9 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64790-65:
(7*6)+(6*4)+(5*7)+(4*9)+(3*0)+(2*6)+(1*5)=154
154 % 10 = 4
So 64790-65-4 is a valid CAS Registry Number.

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64790-65-4Relevant academic research and scientific papers

Cyclohexadiene-trans-diols as versatile starting material in natural product synthesis: Short and efficient synthesis of iso-crotepoxide and ent-senepoxide

Lorbach, Volker,Franke, Dirk,Nieger, Martin,Mueller, Michael

, p. 494 - 495 (2007/10/03)

A new synthesis of ent-senepoxide and iso-crotepoxide starting from microbially produced (+)-trans-2,3-dihydroxy-2,3-dihydrobenzoic acid via regio- and stereoselective epoxidation is described.

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