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905810-22-2

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905810-22-2 Usage

General Description

CHEMBRDG-BB 4024585 is a chemical compound with the chemical formula C20H12N4O3S. It is a benzothiazole-based compound with potential anti-cancer activity. It has been studied for its potential in inhibiting the growth and proliferation of cancer cells. Research has also suggested that it may effectively induce apoptosis in certain cancer cell lines. CHEMBRDG-BB 4024585 has been the subject of interest for its potential as a therapeutic agent in the treatment of cancer, and further studies are being conducted to explore its anti-cancer properties and potential applications in oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 905810-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,8,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 905810-22:
(8*9)+(7*0)+(6*5)+(5*8)+(4*1)+(3*0)+(2*2)+(1*2)=152
152 % 10 = 2
So 905810-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18BrNO/c1-2-9(11)10(13)12-8-6-4-3-5-7-8/h8-9H,2-7H2,1H3,(H,12,13)

905810-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N-cyclohexylbutanamide

1.2 Other means of identification

Product number -
Other names -

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:905810-22-2 SDS

905810-22-2Relevant articles and documents

Transition-Metal-Free Coupling of Alkynes with α-Bromo Carbonyl Compounds: An Efficient Approach towards β,γ-Alkynoates and Allenoates

Liu, Wenbo,Chen, Zhengwang,Li, Lu,Wang, Haining,Li, Chao-Jun

supporting information, p. 5888 - 5893 (2016/04/26)

A direct transition-metal-free coupling between alkynes and α-bromo carbonyl compounds has been developed with ultraviolet (UV) light in aqueous media. This method represents a facile approach to synthetically useful β,γ-alkynyl esters and amides stereoselectively from two readily available starting materials. As an example of the synthetic application of the products, the alkynyl esters were readily converted into allenoates. Time for UV! A direct coupling between alkynes and α-bromo compounds has been developed with ultraviolet light in aqueous media (see scheme). This method represents a facile approach to synthetically useful β,γ-alkynyl esters and amides stereoselectively from two readily available starting materials.

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