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5(2H)-Isoxazolone, 2,3,4-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57892-29-2

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57892-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57892-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,9 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57892-29:
(7*5)+(6*7)+(5*8)+(4*9)+(3*2)+(2*2)+(1*9)=172
172 % 10 = 2
So 57892-29-2 is a valid CAS Registry Number.

57892-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4-triphenyl-1,2-oxazol-5-one

1.2 Other means of identification

Product number -
Other names 3,4,5-triphenyl-4-oxazolin-2-one-4

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:57892-29-2 SDS

57892-29-2Relevant academic research and scientific papers

Synthesis and properties of carbamoyl derivatives of photolabile benzoins

Papageorgiou, George,Corrie, John E.T.

, p. 3917 - 3932 (2007/10/03)

Carbamoyl derivatives of photolabile benzoins, particularly of 3',5'-dimethoxybenzoin, are readily prepared via the mixed p-nitrophenyl carbonate of the benzoin. The method is most suitable for secondary amines, since many primary amines exist in varying proportions as the cyclic In alkaline solution (0.2 M NaOH) the carbamates of unsymmetrical benzoins are readily equilibrated. Flash photolysis of 3',5'-dimethoxybenzoin carbamates generates the carbamate anion in a fast heterolytic process and liberation of the amine is controlled by the rate of decarboxylation.

Skeletal Rearrangement of N,O-Heterocycles. The Isoxazolinone to Aziridine Transformation Induced by Lithium Aluminium Hydride

Chidichimo, G.,Cum, G.,Lelj, F.,Sindona, G.,Uccella, N.

, p. 1372 - 1377 (2007/10/02)

Triphenylisoxazolinone reacts with lithium aluminium hydride to yield either triphenylaziridinic derivatives or open-ring products or both depending on reaction conditions.The structures of the products were ascertained by spectroscopic methodes and their

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