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2952-05-8

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2952-05-8 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 92, p. 6594, 1970 DOI: 10.1021/ja00725a035Synthesis, p. 35, 1976Tetrahedron Letters, 17, p. 4003, 1976

Check Digit Verification of cas no

The CAS Registry Mumber 2952-05-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2952-05:
(6*2)+(5*9)+(4*5)+(3*2)+(2*0)+(1*5)=88
88 % 10 = 8
So 2952-05-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H13N/c1-3-7-12(8-4-1)14-11-15(14)13-9-5-2-6-10-13/h1-10,14H,11H2

2952-05-8SDS

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 1,2-diphenylaziridine

1.2 Other means of identification

Product number -
Other names Aziridine,1,2-diphenyl

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:2952-05-8 SDS

2952-05-8Relevant articles and documents

Thermal azide-Alkene cycloaddition reactions: straightforward multi-gram access to Δ2-1,2,3-Triazolines in deep eutectic solvents

Sebest, Filip,Casarrubios, Luis,Rzepa, Henry S.,White, Andrew J. P.,Díez-González, Silvia

supporting information, p. 4023 - 4035 (2018/09/11)

The multi-gram synthesis of a wide range of 1,2,3-Triazolines via azide-Alkene cycloaddition reactions in a Deep Eutectic Solvent (DES) is reported. The role of DES in this transformation as well as the origin of the full product distribution was studied with an experimental/computational-DFT approach.

A lithiomethyl trimethylammonium reagent as a methylene donor

Den Hartog, Tim,Sarria Toro, Juan M.,Couzijn, Erik P. A.,Chen, Peter

supporting information, p. 10604 - 10607 (2014/11/08)

Straightforward deprotonation of soluble tetramethylammonium salts with alkyllithium reagents gives lithiomethyl trimethylammonium reagents. Coordination of the Li cation is crucial to the stability of these 'N-C ylides'. These reagents were used to prepare epoxides, aziridines and allylic alcohols. This journal is the Partner Organisations 2014.

Novel aziridination of α-halo ketones: an efficient nucleophile-induced cyclization of phosphoramidates to functionalized aziridines

Yadav, Lal Dhar S.,Rai, Ankita,Rai, Vijai K.,Awasthi, Chhama

, p. 687 - 690 (2008/09/17)

A novel and efficient aziridination of α-halo ketones is reported. The reaction of α-halo ketones with diethyl N-arylphosphoramidates affords diethyl N-aryl-N-(2-oxoalkyl)phosphoramidates which undergo reductive (H--induced) cyclization with so

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