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Benzene, 1-[bromo(4-chlorophenyl)methyl]-2-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61023-86-7

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61023-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61023-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,2 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61023-86:
(7*6)+(6*1)+(5*0)+(4*2)+(3*3)+(2*8)+(1*6)=87
87 % 10 = 7
So 61023-86-7 is a valid CAS Registry Number.

61023-86-7SDS

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 1-[bromo-(2-chlorophenyl)methyl]-4-chlorobenzene

1.2 Other means of identification

Product number -
Other names 2,4'-dichlorodiphenyl bromomethane

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:61023-86-7 SDS

61023-86-7Downstream Products

61023-86-7Relevant academic research and scientific papers

Synthesis and anticonvulsant activity of some cinnamylpiperazine derivatives

Hu, Chuan,Sun, Zhi-Gang,Wei, Cheng-Xi,Quan, Zhe-Shan

scheme or table, p. 661 - 664 (2011/11/29)

A series of cinnamylpiperazine derivatives was synthesized using different benzophenone as starting material. The structures of the compounds were proved by their IR, 1H-NMR spectroscopic data and mass spectra data. The anticonvulsant activities of these compounds were evaluated with maximal electroshock (MES) test and rotarod test with intraperitoneal injection on KunMing mice. Among all the flunarizine analogues, no one exhibited better anticonvulsant activity than flunarizine. Flunarizine (4i) exhibited anticonvulsant activity with ED50 of 38.1 mg/kg, TD50 of 164.3 mg/kg and PI of 4.3 through administration intraperitoneal, and with ED50 of 56.8 mg/kg, TD50 of 456.3 mg/kg and PI of 8.0 through oral administration.

Process for the preparation of substituted arylcyanoalkyl and diaryl cyanoalkylimidazoles

-

, (2008/06/13)

This invention relates to a process for the preparation of substituted arylcyanoalkyl and diarylcyanoalkylimidazoles, their acid addition salts and their metal salt complexes. These compounds are useful as broad spectrum protectant-eradicant fungicides.

Substituted arylcyanoalkyl and diarylcyanoalkylimidazoles and fungical compositions and methods utilizing them

-

, (2008/06/13)

This invention relates to substituted arylcyanoalkyl and diarylcyanoalkylimidazoles, their acid addition salts and their metal salt complexes and their use as broad spectrum protectant-eradicant fungicides.

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