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660450-79-3

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660450-79-3 Usage

Structure

Substituted benzophenone containing a bromine atom and two fluorine atoms on the benzene ring.

Primary Use

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

Potential Application

Investigated for use as a photoinitiator in the production of polymeric materials.

UV Absorption

Known for its ability to absorb ultraviolet light, significant in photophysics and photochemistry.

Hazards

Requires careful handling as it can be hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 660450-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,0,4,5 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 660450-79:
(8*6)+(7*6)+(6*0)+(5*4)+(4*5)+(3*0)+(2*7)+(1*9)=153
153 % 10 = 3
So 660450-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H8BrF2NO/c14-7-4-5-11(17)8(6-7)13(18)12-9(15)2-1-3-10(12)16/h1-6H,17H2

660450-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-5-bromophenyl)-(2,6-difluorophenyl)methanone

1.2 Other means of identification

Product number -
Other names (2-amino-5-bromophenyl)(2,6-difluorophenyl)methanone

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:660450-79-3 SDS

660450-79-3Downstream Products

660450-79-3Relevant articles and documents

BENZODIAZEPINE DERIVATIVES AS GABA A GAMMA1 PAM

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Paragraph 0451; 0454, (2021/10/11)

Compounds having the general formula (I) wherein R1, R2, R3, R4, R5 and X are as described herein, compositions including the compounds and methods of using the compounds.

FUSED HETEROCYCLIC COMPOUNDS

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Page 175-176, (2008/06/13)

A compound represented by the formula wherein ring A is an optionally substituted 5- to 10-membered aromatic ring; R1 and R2 are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; X and Y are the same or different and each is a bond, -O-, -S-, -SO-, -SO?2#191- or -NR3- (R3 is a hydrogen atom or an optionally substituted hydrocarbon group); and L is a divalent hydrocarbon group, or a salt thereof shows a superior peptidase-inhibitory activity and is useful as a prophylactic or therapeutic agent of diabetes and the like.

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