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7363-25-9

7363-25-9

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7363-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7363-25-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7363-25:
(6*7)+(5*3)+(4*6)+(3*3)+(2*2)+(1*5)=99
99 % 10 = 9
So 7363-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO4/c1-20-15-11-8-18-5-4-17(3-2-10(19)6-14(17)18)12(11)7-13-16(15)22-9-21-13/h2-3,7,10,14,19H,4-6,8-9H2,1H3/t10-,14+,17+/m0/s1

7363-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Crinan-3-ol,1,2-didehydro-7-methoxy-,(3alpha)

1.2 Other means of identification

Product number -
Other names Powellin

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:7363-25-9 SDS

7363-25-9Downstream Products

7363-25-9Relevant articles and documents

Bioinspired enantioselective synthesis of crinine-type alkaloids: Via iridium-catalyzed asymmetric hydrogenation of enones

Zuo, Xiao-Dong,Guo, Shu-Min,Yang, Rui,Xie, Jian-Hua,Zhou, Qi-Lin

, p. 6202 - 6206 (2017/08/29)

A bioinspired enantioselective synthesis of crinine-type alkaloids has been developed by iridium-catalyzed asymmetric hydrogenation of racemic cycloenones. The method features a biomimetic stereodivergent resolution of the substrates bearing a remote arylated quaternary stereocenter. Using this protocol, 24 crinine-type alkaloids and 8 analogues were synthesized in a concise and rapid way with high yield and high enantioselectivity.

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