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84396-05-4

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84396-05-4 Usage

General Description

"2-[4-(1H-benzimidazol-2-yl)phenoxy]ethyl 4-methylbenzenesulfonate" is a chemical compound with the molecular formula C23H22N2O4S. It consists of a benzimidazole group and a phenoxyethyl group attached to a 4-methylbenzenesulfonate moiety. 2-[4-(1H-benzimidazol-2-yl)phenoxy]ethyl 4-methylbenzenesulfonate is commonly used in pharmaceutical research as a potential drug candidate due to its unique structure and potential pharmacological properties. Additionally, it may also have applications in the field of organic synthesis and material science. Further studies and research are needed to fully understand the potential uses and properties of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 84396-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,9 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84396-05:
(7*8)+(6*4)+(5*3)+(4*9)+(3*6)+(2*0)+(1*5)=154
154 % 10 = 4
So 84396-05-4 is a valid CAS Registry Number.

84396-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(1H-benzimidazol-2-yl)phenoxy]ethyl 4-methylbenzenesulfonate

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

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More Details:84396-05-4 SDS

84396-05-4Downstream Products

84396-05-4Relevant articles and documents

Potential alkylating agents derived from benzimidazole and benzothiazole

Omar,Habib,Aboulwafa

, p. 991 - 993 (2007/10/02)

Several benzimidazole and benzothiazole alkylating agents, bearing structural modification of certain drugs, were synthesized and evaluated for anticancer activity. Among the products, the dihydrochloride salt of 2-{p-[2-(bis(2-chloroethyl)amino)ethoxy]ph

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