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1H-Pyrrole-2,3-dicarboxylic acid, 5-benzoyl-2,3-dihydro-1-hydroxy-4-phenyl-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

488150-29-4

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488150-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 488150-29-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,1,5 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 488150-29:
(8*4)+(7*8)+(6*8)+(5*1)+(4*5)+(3*0)+(2*2)+(1*9)=174
174 % 10 = 4
So 488150-29-4 is a valid CAS Registry Number.

488150-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 5-benzoyl-4-phenyl-1-hydroxy-2,3-dihydropyrrole-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 5-Benzoyl-1-hydroxy-4-phenyl-2,3-dihydro-1H-pyrrole-2,3-dicarboxylic acid diethyl ester

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:488150-29-4 SDS

488150-29-4Downstream Products

488150-29-4Relevant academic research and scientific papers

A comparison of phosphonium and phosphonate carbanion reagents in reactions with 1,3-diphenyl-2-(hydroxyimino)-1,3-propanedione

Abdou, Wafaa M.,El-Khoshnieh, Yehia O.,Salem, Mounir A. I.,Barghash, Reham F.

, p. 1417 - 1422 (2007/10/03)

1,3-Diphenyl-2-(hydroxyimino)-1,3-propanedione 1 reacted with phosphonium ylides 2a,b to give mainly the substituted 1-hydroxy-2,3-dihydropyrroles 6a,b along with the novel ylides 10a,b whereas the phosphono substituted-N-heterocycles 11a,b and 14a,b were obtained from the reaction of 1 with α-phosphoryl carbanion counterparts 3a,b. Reaction of 1 with cyanomethylene(triphenyl)phosphorane 2c afforded the Wittig product 17 and the oxazole derivative 18 while the phosphono 2,2-disubstituted dihydrooxazole 20 and the diolefin 19 were produced in the reaction with the phosphonate ylide 3c. Application of the unsaturated carbanions 2d and 3d on 1 yielded the pyrrole 23 and the phosphono substituted 2H-1,4-oxazine 25, respectively.

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