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Acetic acid, [[1-(4-nitrophenyl)-3-oxo-3-phenylpropyl]thio]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55483-99-3

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55483-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55483-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,8 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55483-99:
(7*5)+(6*5)+(5*4)+(4*8)+(3*3)+(2*9)+(1*9)=153
153 % 10 = 3
So 55483-99-3 is a valid CAS Registry Number.

55483-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[1-(4-nitrophenyl)-3-oxo-3-phenylpropyl]sulfanylacetate

1.2 Other means of identification

Product number -
Other names -

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:55483-99-3 SDS

55483-99-3Downstream Products

55483-99-3Relevant academic research and scientific papers

Fluorapatite: Efficient catalyst for the Michael addition

Zahouily, Mohamed,Abrouki, Younes,Rayadh, Ahmed,Sebti, Sa?d,Dhimane, Hamid,David, Marc

, p. 2463 - 2465 (2003)

A Michael addition assisted by fluorapatite in heterogeneous media is described. Reaction between mercaptans and chalcone derivatives was studied at room temperature in methanol as solvent. By-products of usual undesirable reactions in Michael addition su

Stereochemical studies of Michael-adducts obtained by reaction of the ethyl mercaptoacetate with substituted propenones and of their cyclisation into ethyl 3-hydroxytetrahydrothiophene-2-carboxylates.

Robert, J. F.,Xicluna, A.,Ombetta, J. E.,Alhassan, M.,Mercier, M. F.,et al.

, p. 478 - 485 (2007/10/02)

A conformational study of several Michael-adducts issued from the reaction of ethyl mercaptoacetate with substituted propenones was carried out in order to understand the remarkable stereospecificity of their cyclization into tetrahydrothiophene derivativ

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