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968-02-5

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968-02-5 Usage

Type of compound

Three-membered heterocyclic compound

Presence of nitrogen

Contains a nitrogen atom in its ring structure

Physical state

Colorless to pale yellow liquid

Molecular weight

262.35 g/mol

Usage

Chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Reactivity

Highly reactive, capable of undergoing nucleophilic addition reactions

Application

Chiral building block in the synthesis of biologically active molecules

Safety precautions

Handle with caution due to potential toxicity, skin and eye irritation, and inhalation risks

Check Digit Verification of cas no

The CAS Registry Mumber 968-02-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 968-02:
(5*9)+(4*6)+(3*8)+(2*0)+(1*2)=95
95 % 10 = 5
So 968-02-5 is a valid CAS Registry Number.

968-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3-triphenylaziridine

1.2 Other means of identification

Product number -
Other names 1,2,3-triphenyl-3-methoxycyclopropene

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:968-02-5 SDS

968-02-5Relevant articles and documents

Aziridine synthesis in the presence of catalytic amounts of pyridiniums or viologens

Xue, Zheng,Mazumdar, Arindam,Hope-Weeks, Louisa J.,Mayer, Michael F.

, p. 4601 - 4603 (2008/09/21)

Pyridinium and viologen species were found to induce an aziridine-forming reaction from various imines and phenyldiazomethane. The reactions were generally high yielding and demonstrated cis-aziridine selectivity.

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