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78287-26-0

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78287-26-0 Usage

Chemical Properties

Yellow Solid

Uses

Different sources of media describe the Uses of 78287-26-0 differently. You can refer to the following data:
1. Camptothecin analog as DNA topoisomerase I inhibitors: a QSAR study. It may also be useful in the design and development of new camptothecin derivatives as DNA topoisomerase I (topo I) inhibitors. A poorly water soluble camptothecin analogue. Antitumor agent.
2. 7-Methyl Camptothecin is a poorly water soluble camptothecin analogue. It as DNA topoisomerase I inhibitors: a QSAR study. It may also be useful in the design and development of new camptothecin derivatives as DNA topoisomerase I (topo I) inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 78287-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,2,8 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78287-26:
(7*7)+(6*8)+(5*2)+(4*8)+(3*7)+(2*2)+(1*6)=170
170 % 10 = 0
So 78287-26-0 is a valid CAS Registry Number.

78287-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methylcamptothecin

1.2 Other means of identification

Product number -
Other names 7-Methyl Camptothecin

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:78287-26-0 SDS

78287-26-0Downstream Products

78287-26-0Relevant articles and documents

Novel route for preparation of 7-methyl-camptothecin and its possible mechanism

Wang, Xin,Wen, Jiwu,Li, Gang,You, Tianpa

, p. 3163 - 3166 (2005)

A novel route for preparation of 7-methyl-camptothecin is described. Its possible mechanism is discussed. Copyright Taylor & Francis, Inc.

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