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37763-43-2

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37763-43-2 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 14, p. 375, 1949 DOI: 10.1021/jo01155a006

Check Digit Verification of cas no

The CAS Registry Mumber 37763-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,6 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37763-43:
(7*3)+(6*7)+(5*7)+(4*6)+(3*3)+(2*4)+(1*3)=142
142 % 10 = 2
So 37763-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H8Br2/c12-7-9-6-5-8-3-1-2-4-10(8)11(9)13/h1-6H,7H2

37763-43-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H50240)  1-Bromo-2-(bromomethyl)naphthalene, 98%   

  • 37763-43-2

  • 250mg

  • 682.0CNY

  • Detail
  • Alfa Aesar

  • (H50240)  1-Bromo-2-(bromomethyl)naphthalene, 98%   

  • 37763-43-2

  • 1g

  • 1241.0CNY

  • Detail

37763-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-2-(BROMOMETHYL)NAPHTHALENE

1.2 Other means of identification

Product number -
Other names 1-Bromo-2-bromomethyl-naphthalene

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:37763-43-2 SDS

37763-43-2Relevant articles and documents

Selective benzylic bromination of 2-methylnaphthalene

Waykole, Liladhar,Prashad, Mahavir,Palermo, Stephen,Repic, Oljan,Blacklock, Thomas J.

, p. 2159 - 2163 (2007/10/03)

A practical synthesis of 2-(bromomethyl)naphthalene (1) by selective benzylic bromination of 2-methylnaphthalene (2) with bromine in heptane in the presence of lanthanum acetate hydrate is described.

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