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14704-31-5

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14704-31-5 Usage

Chemical Properties

offwhite to light yellow crystal powder

Uses

3-Phenylbenzyl bromide may be used in the synthesis of the following amino alcohols:NH-benzyl-(1R,2S)-norephedrineNH-3-phenylbenzyl-(1R,2S)-norephedrine(1R,2S)-2-(benzylamino)-1,2-diphenylethanol

Check Digit Verification of cas no

The CAS Registry Mumber 14704-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,0 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14704-31:
(7*1)+(6*4)+(5*7)+(4*0)+(3*4)+(2*3)+(1*1)=85
85 % 10 = 5
So 14704-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H11Br/c14-10-11-5-4-8-13(9-11)12-6-2-1-3-7-12/h1-9H,10H2

14704-31-5SDS

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 3-(Bromomethyl)biphenyl

1.2 Other means of identification

Product number -
Other names 3-(Bromomethyl)-1,1'-biphenyl

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:14704-31-5 SDS

14704-31-5Relevant articles and documents

Triazolone derivatives, use thereof, and intermediates therefor

-

, (2008/06/13)

Triazolone derivatives represented by the formula wherein R1represents optionally substituted C1-10alkyl, A1—L1—, A1—ON═CA2, etc.; R2represents hydrogen, C1-6alkyl, etc.; R3represents C1-6alkoxy, etc.; one of T, U, and V represents CR4, another represents CH or nitrogen, and the remaining one represents CR5or nitrogen; and W represents CR6or nitrogen.

Synthesis of aryl(difluoromethylenephosphonates) via electrophilic fluorination of α-carbanions of benzylic phosphonates with N- fluorobenzenesulfonimide.

Taylor, Scott D.,Kotoris, Christopher C.,Dinaut, A. Nicole,Chen, Mei-Jin

, p. 1691 - 1714 (2007/10/03)

The electrophilic fluorination of a wide variety of benzylic phosphonates with N-fluorobenzenesulfonimide has been examined. The fluorination reaction proceeds well in the presence of an array of functional groups such as nitro, bromo, ketone, ester, phenyl and ether groups. Phenyl and biphenyl derivatives containing two α,α-difluoromethylenephosphonate groups can also be prepared. This procedure is compatible with methyl or ethyl phosphonate esters but not with t-butyl esters or with benzylic phosphonates containing an additional benzylic moiety at the para-position.

Insecticidal 5-substituted-2,4-diaminopyrimidine derivatives

-

, (2008/06/13)

An insecticidal composition comprising, in admixture with an agriculturally acceptable carrier, an insecticidally effective amount of a compound of the formula: STR1 wherein R, R1, R2, R3, R7, R8, m, n, and p are as defined herein, and agriculturally acceptable salts thereof, and methods of using the same.

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