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1,2,3-triphenylaziridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34310-77-5

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34310-77-5 Usage

Chemical class

Aziridines

Ring size

Three-membered

Ring composition

Contains nitrogen

Use

Precursor in the synthesis of various organic compounds

Applications

Pharmaceutical and agrochemical industries

Importance

Building block in organic chemistry

Utilization

Manufacturing of fine chemicals

Biological activities

Studied for potential applications

Asymmetric synthesis

Used as a chiral auxiliary

Chemical structure

Unique and valuable in organic synthesis and medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 34310-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,1 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34310-77:
(7*3)+(6*4)+(5*3)+(4*1)+(3*0)+(2*7)+(1*7)=85
85 % 10 = 5
So 34310-77-5 is a valid CAS Registry Number.

34310-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 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:34310-77-5 SDS

34310-77-5Relevant academic research and scientific papers

PHOTOFRAGMENTATION OF OXAZOLIDINES. A NEW METHOD FOR THE GENERATION OF AZIRIDINES

Tsuge, Otohiko,Oe, Koji,Kawaguchi, Noriyuki

, p. 1585 - 1588 (2007/10/02)

Irradiation of 4,5-cis-2,3,4,5-tetraaryloxazolidines and 3-aryl-3a,9b-dihydro-acenaphthoxazolidines generates the corresponding aziridine intermediates with elimination of aldehyde formed by fission of the C2-O and C4-C5 bonds in the former and the C2-O and C2-N bonds int the latter, respectively.The intervention of aziridine intermediates was proved by photo-cycloadditions.

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