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Benzenamine, 2-[2-(2-chlorophenyl)ethenyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62640-64-6

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62640-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62640-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,4 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62640-64:
(7*6)+(6*2)+(5*6)+(4*4)+(3*0)+(2*6)+(1*4)=116
116 % 10 = 6
So 62640-64-6 is a valid CAS Registry Number.

62640-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-2'-chlorostilbene

1.2 Other means of identification

Product number -
Other names 2-Chlor-2'-aminostilben

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:62640-64-6 SDS

62640-64-6Downstream Products

62640-64-6Relevant academic research and scientific papers

DMSO/SOCl2-mediated C(sp2)-H amination: Switchable synthesis of 3-unsubstituted indole and 3-methylthioindole derivatives

Zhang, Jingran,Li, Xiaoxian,Li, Xuemin,Shi, Haofeng,Sun, Fengxia,Du, Yunfei

, p. 460 - 463 (2021)

The reaction of 2-alkenylanilines with SOCl2 in DMSO was found to selectively afford 3-unsubstituted indoles and 3-methylthioindoles. This switchable approach was found to be temperature-dependent: at room temperature, the reaction afforded 3-unsubstituted indoles through intramolecular cyclization and elimination; while at higher temperature, the reaction gave 3-methylthioindoles via further electrophilic methylthiolation.

N-phenylcarbamate compound, process for preparing the sasme and biocidal composition for control of harmful organisms

-

, (2008/06/13)

A novel N-phenylcarbamate compound or its salt where possible, which is useful as the active ingredient of a biocidal composition for control of harmful organisms, is represented by the following general formula (I): STR1 wherein R1 is unsubsti

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