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6-broMo-3-(4-broMophenyl)-3,4-dihydroquinazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65331-45-5

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65331-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65331-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,3 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65331-45:
(7*6)+(6*5)+(5*3)+(4*3)+(3*1)+(2*4)+(1*5)=115
115 % 10 = 5
So 65331-45-5 is a valid CAS Registry Number.

65331-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-3-(4-bromophenyl)-4H-quinazoline

1.2 Other means of identification

Product number -
Other names 6-bromo-3-(4-bromophenyl)-3,4-dihydroquinazoline

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:65331-45-5 SDS

65331-45-5Relevant academic research and scientific papers

Mild environment-friendly oxidative debenzylation of N-benzylanilines using DMSO as an oxidant

Yoshinaga, Tatsuro,Iwata, Takayuki,Shindo, Mitsuru

supporting information, p. 191 - 194 (2020/02/25)

Oxidative debenzylation of N-benzyl aromatic amines using DMSO as a non-toxic oxidant and catalyzed by TsOH gave Nphenylimines, which were spontaneously hydrolyzed to form anilines and benzaldehydes in good yields. This reaction employs mild, metal-free conditions. The conditions are also suitable for the debenzylation of benzylphenylethers.

Two isolated intermediates of the Tr?ger's base: synthesis and mechanism

Wan, Yu,Yuan, Rui,Zhang, Wei-chao,Shi, Yan-hui,Lin, Wei,Yin, Wei,Bo, Rong-cheng,Shi, Jing-jing,Wu, Hui

experimental part, p. 3405 - 3409 (2010/06/21)

By controlling the amount of catalyst 1-methyl-3-(2-(sulfooxy)ethyl)-1H-imidazol-3-ium chloride, two new intermediates of Tr?ger's bases (11, 1,6-dimethyl-3-(4-methylphenyl)-1,4-dihydroquinazolin-3-ium tetrafluoroborate and 12, 8-methyl-2,5-bis-(4-methylp

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