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28910-83-0

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28910-83-0 Usage

Chemical Properties

Yellow Solid

Uses

2-Aminobenzophenone derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 28910-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,1 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28910-83:
(7*2)+(6*8)+(5*9)+(4*1)+(3*0)+(2*8)+(1*3)=130
130 % 10 = 0
So 28910-83-0 is a valid CAS Registry Number.

28910-83-0SDS

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-5-chlorophenyl)-(2,6-difluorophenyl)methanone

1.2 Other means of identification

Product number -
Other names 2-Amino-5-chloro-2',6'-difluorobenzophenon

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:28910-83-0 SDS

28910-83-0Relevant articles and documents

Bioorthogonal imaging of Aurora Kinase A in live cells

Yang, Katherine S.,Budin, Ghyslain,Reiner, Thomas,Vinegoni, Claudio,Weissleder, Ralph

supporting information; experimental part, p. 6598 - 6603 (2012/09/22)

In living color: Aurora kinase A (AKA) was imaged in live cells using a bioorthogonal two-step reaction with a small molecule AKA inhibitor (see scheme) and a fluorescent reporter. The fluorescent molecule was localized to spindle poles and microtubules d

2-(2-Alkynylamino)-3H-1,4-benzodiazepines

-

, (2008/06/13)

Novel 6-substituted 4H-imidazo[1,2-a][1,4]benzodiazepines, the intermediate 5-substituted-2-(2-alkynylamino)-3H-1,4-benzodiazepines, pharmacologically acceptable acid addition salts thereof, and processes for their production. The compounds of this invention and the pharmacologically acceptable acid addition salts thereof are central nervous system depressants. They are useful as sedatives, hypnotics, tranquilizers, muscle relaxants and anticonvulsants, and also as feed additives for increasing growth rate and feed efficiency of livestock and poultry, milk production in the mammalian species and egg production in avian species.

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