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6962-03-4

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6962-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6962-03-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6962-03:
(6*6)+(5*9)+(4*6)+(3*2)+(2*0)+(1*3)=114
114 % 10 = 4
So 6962-03-4 is a valid CAS Registry Number.

6962-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(7S)-10-(diethylamino)-1,2,3-trimethoxy-9-oxo-6,7-dihydro-5H-benzo[a]heptalen-7-yl]acetamide

1.2 Other means of identification

Product number -
Other names COLCHICINE,10-DEMETHOXY-10-(DIETHYLAMINO)

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:6962-03-4 SDS

6962-03-4Downstream Products

6962-03-4Relevant articles and documents

Synthesis, antiproliferative and antibacterial evaluation of C-ring modified colchicine analogues

Huczyński, Adam,Rutkowski, Jacek,Popiel, Katarzyna,Maj, Ewa,Wietrzyk, Joanna,Stefańska, Joanna,Majcher, Urszula,Bartl, Franz

, p. 296 - 301 (2015)

A series of 10 amine derivatives of colchicine have been obtained with high yields by modification at C(10)-OCH3position of C-ring and characterized by spectroscopic methods. In vitro cytotoxicity has been evaluated against four human tumour ce

Synthesis and antitumour activity of novel colchicine C-10 derivatives

Shen, Li Hong,Zhang, Le,Wang, Hai Xian,Wang, Xin,Zhang, Gai Jiao

, p. 7475 - 7476 (2015/04/22)

A series of new colchicine C-10 derivatives (2a-i, 3a-h) were synthesized by replacement of the 10-methoxy with NR2 and SCH3 in order to determine their cytotoxic activity. The compounds were synthesized in good yield and the structures of all newly synthesized compounds were established on the basis of their IR, 1H NMR and elemental analysis. The synthesized compounds were tested in vitro antitumor activity against four human cancer cell lines by MTT assay. It was found that many of the derivatives displayed significant activity, particularly, compound 2a and 2b showed more potent cytotoxic activities than colchicine.

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