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1617-93-2

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1617-93-2 Usage

Chemical structure

An oxadiazole derivative with a substituted phenylethyl group at the 5-position

Potential applications

Pharmaceutical and agrochemical industries

Biological activities

May exhibit various biological activities due to its unique structure and chemical properties

Research and development

Of interest for further research and development

Safety protocols

Important to handle with care and in accordance with proper safety protocols due to potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 1617-93-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1617-93:
(6*1)+(5*6)+(4*1)+(3*7)+(2*9)+(1*3)=82
82 % 10 = 2
So 1617-93-2 is a valid CAS Registry Number.

1617-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(2-phenylethyl)-1,3,4-oxadiazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-5-(2-phenyl-aethyl)-1,3,4-oxadiazol

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:1617-93-2 SDS

1617-93-2Relevant articles and documents

Synthesis of N-pyrimidin[1,3,4]oxadiazoles and N-pyrimidin[1,3,4]-thiadiazoles from 1,3,4-oxadiazol-2-amines and 1,3,4-thiadiazol-2-amines via Pd-catalyzed heteroarylamination

Yan, Longjia,Deng, Minggao,Chen, Anchao,Li, Yongliang,Zhang, Wanzheng,Du, Zhi-yun,Dong, Chang-zhi,Meunier, Bernard,Chen, Huixiong

supporting information, p. 1359 - 1362 (2019/04/25)

An efficient and practical procedure was developed to prepare various N-pyrimidin[1,3,4]oxadiazole and thiadiazole scaffolds using a Buchwald-type coupling. The products of this reaction are otherwise difficult to access and could be used as building bloc

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