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24345-72-0

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24345-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24345-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24345-72:
(7*2)+(6*4)+(5*3)+(4*4)+(3*5)+(2*7)+(1*2)=100
100 % 10 = 0
So 24345-72-0 is a valid CAS Registry Number.

24345-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-diazidobutane

1.2 Other means of identification

Product number -
Other names Butane,1,4-diazido

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:24345-72-0 SDS

24345-72-0Upstream product

24345-72-0Downstream Products

24345-72-0Relevant articles and documents

Solution-phase parallel synthesis and screening of anti-tumor activities from fenbufen and ethacrynic acid libraries

Su, Yuan-Hsiao,Chiang, Li-Wu,Jeng, Kee-Ching,Huang, Ho-Lien,Chen, Jenn-Tzong,Lin, Wuu-Jyh,Huang, Chia-Wen,Yu, Chung-Shan

, p. 1320 - 1324 (2011)

The derivatives with fenbufen and ethacrynic acid core compounds was synthesized through a facial preparation of 1-amino-4-azidobutane. The subsequent coupling with 102 members of carboxylic acids afforded amide products. The in situ screening using colorimetric assay with 3-(4.5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide showed that fenbufen but not ethacrynic acid butyl amide members displayed the cytotoxicities to tumor cells substantially, including two human cell lines (MCF7 and A549) and two murine cell lines (C26 and TRAMP-C1). Three fenbufen analogs were found to have a good anti-tumor activity comparable to cisplatin.

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