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1316275-31-6

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1316275-31-6 Usage

Uses

2-Bromoquinazoline is a useful reagent in the preparation of triphenylene-?based polycyclic aromatic hydrocarbons (PAHs) from ring-?fused benzocyclobutenols (RBCBs) via the cleavage of the C-?C σ-?bond.

Check Digit Verification of cas no

The CAS Registry Mumber 1316275-31-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,6,2,7 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1316275-31:
(9*1)+(8*3)+(7*1)+(6*6)+(5*2)+(4*7)+(3*5)+(2*3)+(1*1)=136
136 % 10 = 6
So 1316275-31-6 is a valid CAS Registry Number.

1316275-31-6SDS

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 bromoquinazoline

1.2 Other means of identification

Product number -
Other names 2-Bromoquinazoline

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:1316275-31-6 SDS

1316275-31-6Upstream product

1316275-31-6Downstream Products

1316275-31-6Relevant articles and documents

A highly practical and convenient halogenation of fused heterocyclic N-oxides

Wang, Dong,Wang, Yuxi,Zhao, Junjie,Li, Linna,Miao, Longfei,Wang, Dong,Sun, Hua,Yu, Peng

, p. 5762 - 5768 (2016/08/30)

A novel, simple and practical method for the regioselective halogenation of fused heterocyclic N-oxides has been developed. It employs Vilsmeier reagent, generated in situ by POX3and DMF, as both the activating agent and the nucleophilic halide source. The method is amenable across a broad range of substrates, including quinolines, isoquinolines and the diazine N-oxides, possessing a variety of substitution patterns. Furthermore, all of the reagents associated are cheap and easy to obtain. The potential extension of this method to a one-pot oxidation/halogenation sequence that obviates the need for isolation of the N-oxide intermediates is also presented.

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