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2-benzyl-1H-perimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28537-43-1

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28537-43-1 Usage

Synthesis Reference(s)

Synthetic Communications, 21, p. 2171, 1991 DOI: 10.1080/00397919108055450

Check Digit Verification of cas no

The CAS Registry Mumber 28537-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,3 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28537-43:
(7*2)+(6*8)+(5*5)+(4*3)+(3*7)+(2*4)+(1*3)=131
131 % 10 = 1
So 28537-43-1 is a valid CAS Registry Number.

28537-43-1SDS

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 2-benzyl-1H-perimidine

1.2 Other means of identification

Product number -
Other names 2-Benzylperimidin

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:28537-43-1 SDS

28537-43-1Downstream Products

28537-43-1Relevant academic research and scientific papers

Synthesis of new perimidine derivatives from the reaction of 1,8-diaminonapthalene with iminoester hydrochlorides

Kahveci, Bahittin,Karaali, Nesrin,Mentese, Emre,Yilmaz, Fatih

, p. 377 - 379 (2013)

An alternative procedure is described for the synthesis of 2-substituted perimidines involving the reaction of 1,8- diaminonapthalene with iminoester hydrochlorides of substituted phenylacetic acids under microwave irradiation. This leads to good yields i

Design, synthesis and biological evaluation of novel perimidine o-quinone derivatives as non-intercalative topoisomerase II catalytic inhibitors

Zhou, Du-Chao,Lu, Yu-Ting,Mai, Yan-Wen,Zhang, Chen,Xia, Jie,Yao, Pei-Fen,Wang, Hong-Gen,Huang, Shi-Liang,Huang, Zhi-Shu

, (2019/08/06)

For the development of novel anticancer agents, we designed and synthesized a total of 37 perimidine o-quinone derivatives containing the o-quinone group at the A or B ring and different substituents (alkyl groups, aryl groups or heterocycles) at the C ri

Synthesis of 2-aralkyl-1H-perimidines

Reddy, R. Rambhupal,Rao, C. V. Chalapathi

, p. 367 - 369 (2007/10/02)

2-Aralkyl-1H-perimidines 3a-g and 4 have been synthesised by the condensation of 2-methyl/phenyl-4-arylidene-2-oxazolin-5-ones (2a-h) with 1,8-diaminonapthalene (1) and also by the pyrolysis of arylacetic acids 5.The structures of these compounds (3a-g an

An improved one-pot method for the preparation of 2-substituted 1H-perimidines

Maquestiau,Berte,Mayence,Vanden Eynde

, p. 2171 - 2180 (2007/10/02)

2-Substituted 1H-perimidines are readily prepared, in high yields, by refluxing a mixture of sodium pyrosulfite, an aldehyde, and 1,8-diaminonapthalene in aqueous ethanol or N,N-dimethylformamide. The method is of wide applicability except from

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