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101156-38-1

101156-38-1

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  • Aspidospermidine-3-carboxylicacid, 4-(acetyloxy)-6,7-didehydro-15-[(3b,5a,7b,12R,19a)-1,2-didehydro-7-ethyl-7-hydroxy-3-(methoxycarbonyl)-20,21-dinoraspidospermidin-3-yl]-1-formyl-3-hydroxy-16-methoxy

    Cas No: 101156-38-1

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101156-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101156-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,1,5 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101156-38:
(8*1)+(7*0)+(6*1)+(5*1)+(4*5)+(3*6)+(2*3)+(1*8)=71
71 % 10 = 1
So 101156-38-1 is a valid CAS Registry Number.

101156-38-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclovincristine

1.2 Other means of identification

Product number -
Other names 4'-acetoxy-2,3'a-diethyl-6'-formyl-2,5'-dihydroxy-8'-methoxy-2,3,3a,11,12,12b,3'a,4',5',5'a,6',11',12',12'b-tetradecahydro-1H,4H,1'H-[5,9']bi[6,12a-diaza-indeno[7,1-cd]fluorenyl]-5,5'-dicarboxylic acid dimethyl ester

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:101156-38-1 SDS

101156-38-1Downstream Products

101156-38-1Relevant articles and documents

Bisindole alkaloids condensed with a cyclopropane ring, part 1. 14,15-cyclopropanovinblastine and - Vincristine

Keglevich, Peter,Hazai, Laszlo,Dubrovay, Zsofia,Dekany, Miklos,Szantay Jr., Csaba,Kalaus, Gyoergy

, p. 653 - 668 (2014/04/03)

A new type of vinblastine and vincristine derivatives was synthesized. The carbon carbon double bond in position 14 and 15 of the vindoline ring was cyclopropanated. In the course of the synthetic work 14,15-cyclopropanovindoline was coupled with catharanthine, resulting in the cyclopropanated anhydrovinblastine as a key intermediate to 14,15-cyclopropano-vinblastine and - vincristine.

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