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38681-90-2

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38681-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38681-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,8 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38681-90:
(7*3)+(6*8)+(5*6)+(4*8)+(3*1)+(2*9)+(1*0)=152
152 % 10 = 2
So 38681-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H24N2O3/c1-11(23)13-10-22-8-7-20-14-5-3-4-6-15(14)21-18(20)17(19(24)25-2)12(13)9-16(20)22/h3-6,11-13,16,21,23H,7-10H2,1-2H3/t11-,12-,13-,16-,20?/m0/s1

38681-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (–)-echitamidine

1.2 Other means of identification

Product number -
Other names Curan-17-oic acid, 2,16-didehydro-19-hydroxy-, methyl ester, (19S)-

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:38681-90-2 SDS

38681-90-2Downstream Products

38681-90-2Relevant articles and documents

Total syntheses of (-)-alstolucines A, B, and F, (-)-echitamidine, and (-)-N-demethylalstogucine

Teijaro, Christiana N.,Zhao, Senzhi,Kokkonda, Praveen,Andrade, Rodrigo B.

, p. 1547 - 1556 (2015)

Abstract The first enantioselective total syntheses of (-)-alstolucinces A, B, and F, (-)-echitamidine, and (-)-N-demethylalstogucine are reported. This article details the development of our first- and second-generation approaches toward the ABCE tetracyclic core of the strychnos alkaloids and the application thereof to the aforementioned targets. Key steps involve our sequential one-pot biscyclization method that constructs the C and E rings of the tetracyclic core and Rawal's application of the intramolecular Heck reaction to secure the pentacyclic framework common amongst all targets.

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