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380650-10-2

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380650-10-2 Usage

Properties

Organic compound, phenyl ring containing two chlorine atoms, carbonyl group attached to amino group

Uses

Synthesis of pharmaceuticals, intermediate in pesticide and herbicide production, building block for other chemical compounds, key ingredient in dye and pigment synthesis

Applications

Laboratory research purposes, not commonly found in consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 380650-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,6,5 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 380650-10:
(8*3)+(7*8)+(6*0)+(5*6)+(4*5)+(3*0)+(2*1)+(1*0)=132
132 % 10 = 2
So 380650-10-2 is a valid CAS Registry Number.

380650-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-(3,4-dichloro-phenyl)-ethanone

1.2 Other means of identification

Product number -
Other names 2-Amino-1-(3,4-dichlor-phenyl)-aethanon

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:380650-10-2 SDS

380650-10-2Relevant articles and documents

7-([1,2,4,]TRIAZOLO[1,5,-A]PYRIDIN-6-YL)-4-(3,4-DICHLOROPHENYL)-1,2,3,4- TETRAHYDROISOQUINOLINE AND USE THEREOF

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Page/Page column 38, (2010/12/17)

Novel [l,2,4]triazolo[l,5-α]pyridinyl-6-yl-substituted tetrahydroisoquinolines are described in the present invention. These compounds and crystalline forms SAl and N-2 are used in the treatment of various neurological and physiological disorders. Methods of making these compounds and crystalline forms SA-I and N-2 are also described in the present invention.

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