Cas 340167-82-0,(7α,7'β,8α,8'α)-3',4'-dihydroxy-3,4-methylenedioxy-7,9':7',9-diepoxylignane

340167-82-0

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Basic information

Product Name: (7α,7'β,8α,8'α)-3',4'-dihydroxy-3,4-methylenedioxy-7,9':7',9-diepoxylignane
Synonyms:
CAS NO:340167-82-0
Molecular Formula:
Molecular Weight: 342.348
EINECS: N/A
Product Categories: N/A
Mol File: 340167-82-0.mol
Article Data: 1

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: (7α,7'β,8α,8'α)-3',4'-dihydroxy-3,4-methylenedioxy-7,9':7',9-diepoxylignane(CAS DataBase Reference)
NIST Chemistry Reference: (7α,7'β,8α,8'α)-3',4'-dihydroxy-3,4-methylenedioxy-7,9':7',9-diepoxylignane(340167-82-0)
EPA Substance Registry System: (7α,7'β,8α,8'α)-3',4'-dihydroxy-3,4-methylenedioxy-7,9':7',9-diepoxylignane(340167-82-0)

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: 340167-82-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 340167-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,0,1,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 340167-82:
(8*3)+(7*4)+(6*0)+(5*1)+(4*6)+(3*7)+(2*8)+(1*2)=120
120 % 10 = 0
So 340167-82-0 is a valid CAS Registry Number.

340167-82-0Upstream product

133-04-0 episesamin

340167-82-0Downstream Products

340167-82-0Relevant articles and documents

Identification of the metabolites of episesamin in rat bile and human liver microsomes

Tomimori, Namino,Nakai, Masaaki,Ono, Yoshiko,Kitagawa, Yoshinori,Kiso, Yoshinobu,Shibata, Hiroshi

, p. 709 - 716 (2012)

Episesamin is an isomer of sesamin, resulting from the refining process of non-roasted sesame seed oil. Episesamin has two methylendioxyphenyl groups on exo and endo faces of the bicyclic skeleton. The side methylendioxyphenyl group was metabolized by cyt

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