Cas 371155-82-7,(3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol 4-monobenzoate

371155-82-7

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Basic information

Product Name: (3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol 4-monobenzoate
Synonyms:
CAS NO:371155-82-7
Molecular Formula:
Molecular Weight: 290.316
EINECS: N/A
Product Categories: N/A
Mol File: 371155-82-7.mol
Article Data: 2

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: (3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol 4-monobenzoate(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol 4-monobenzoate(371155-82-7)
EPA Substance Registry System: (3aS,4R,7R,7aS)-3a,4,7,7a-tetrahydro-2,2-dimethyl-1,3-benzodioxole-4,7-diol 4-monobenzoate(371155-82-7)

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: 371155-82-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 371155-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,1,1,5 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 371155-82:
(8*3)+(7*7)+(6*1)+(5*1)+(4*5)+(3*5)+(2*8)+(1*2)=137
137 % 10 = 7
So 371155-82-7 is a valid CAS Registry Number.

371155-82-7Upstream product

371155-82-7Downstream Products

526-87-4 (1R,2S,3S,4S)-5-cyclohexene-1,2,3,4-tetrol

371155-82-7Relevant articles and documents

Facile synthetic routes to all possible enantiomeric pairs of conduritol stereoisomers via efficient enzymatic resolution of conduritol B and C derivatives

Kwon, Yong-Uk,Chung, Sung-Kee

, p. 3013 - 3015 (2001)

matrix presented The first synthesis of all possible enantiomeric pairs of conduritol stereoisomers has been accomplished by efficient enzymatic resolution of conduritol B and C derivatives, followed by oxidation/reduction and the Mitsunobu reaction in st

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