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732-79-6

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732-79-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 732-79-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 732-79:
(5*7)+(4*3)+(3*2)+(2*7)+(1*9)=76
76 % 10 = 6
So 732-79-6 is a valid CAS Registry Number.

732-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-[4-[bis(2-chloroethyl)amino]phenyl]methylideneamino]thiourea

1.2 Other means of identification

Product number -
Other names 4-[Bis-(2-chlor-aethyl)-amino]-benzaldehyd-thiosemicarbazon

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:732-79-6 SDS

732-79-6Downstream Products

732-79-6Relevant articles and documents

Thiazole-based nitrogen mustards: Design, synthesis, spectroscopic studies, DFT calculation, molecular docking, and antiproliferative activity against selected human cancer cell lines

?aczkowski, Krzysztof Z.,?witalska, Marta,Baranowska-?Aczkowska, Angelika,Plech, Tomasz,Paneth, Agata,Misiura, Konrad,Wietrzyk, Joanna,Czaplińska, Barbara,Mrozek-Wilczkiewicz, Anna,Malarz, Katarzyna,Musio?, Robert,Grela, Izabela

, p. 139 - 150 (2016)

Synthesis, characterization and investigation of antiproliferative activity of ten thiazole-based nitrogen mustard against human cancer cells lines (MV4-11, A549, MCF-7 and HCT116) and normal mouse fibroblast (BALB/3T3) is presented. The structures of novel compounds were determined using 1H and 13C NMR, FAB(+)-MS, and elemental analyses. Among the derivatives, 5b, 5c, 5e, 5f and 5i were found to exhibit high activity against human leukaemia MV4-11 cells with IC50 values of 2.17-4.26 μg/ml. The cytotoxic activity of compound 5c and 5f against BALB/3T3 cells is up to 20 times lower than against cancer cell lines. Our results also show that compounds 5e and 5i have very strong activity against MCF-7 and HCT116 with IC50 values of 3.02-4.13 μg/ml. Moreover, spectroscopic characterization and cellular localization for selected compound were performed. In order to identify potential drug targets we perform computer simulations with DNA-binding site of hTopoI and hTopoII and quantum chemical calculation of interaction and binding energies in complexes of the five most active compounds with guanine.

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