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147512-46-7

147512-46-7

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147512-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147512-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,1 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 147512-46:
(8*1)+(7*4)+(6*7)+(5*5)+(4*1)+(3*2)+(2*4)+(1*6)=127
127 % 10 = 7
So 147512-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H28O7/c1-19-8-16(23)15(22)7-11(19)3-5-13-14(19)6-4-12-9-26-20(2)21(12,25)17(10-27-20)28-18(13)24/h3,9,13-17,22-23,25H,4-8,10H2,1-2H3

147512-46-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Hancogenin B

1.2 Other means of identification

Product number -
Other names 17-Hydroxygylaucogenin A

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:147512-46-7 SDS

147512-46-7Downstream Products

147512-46-7Relevant articles and documents

Cynanosides A-J, ten novel pregnane glycosides from Cynanchum atratum

Bai, Hong,Li, Wei,Koike, Kazuo,Satou, Tadaaki,Chen, Yingjie,Nikaido, Tamotsu

, p. 5797 - 5811 (2007/10/03)

Four novel 13,14:14,15-diseco-18-nor-pregnane-type steroidal glycosides, cynanosides A-D (1-4), and six novel 13,14:14,15-diseco-pregnane-type steroidal glycosides, cynanosides E-J (5-10) were isolated from the roots of Cynanchum atratum, together with one known compound, cynatratoside F (11). Their structures including the absolute stereochemistry were determined on the basis of spectroscopic analysis and chemical evidence, with combination of the modified Mosher method, the exciton chirality method and chemical transformations.

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