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Diethyl (acetylamino)(3-oxo-3-phenylpropyl)propanedioate is a complex organic compound with the chemical formula C21H25NO5. It is a derivative of propanedioic acid, featuring an acetylamino group and a 3-oxo-3-phenylpropyl moiety. diethyl (acetylamino)(3-oxo-3-phenylpropyl)propanedioate is characterized by its ester linkages to two ethyl groups and a central propanedioic acid backbone. It is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. The compound's structure allows for a range of chemical reactions, making it a versatile intermediate in organic synthesis. Its specific applications and properties are determined by its ability to form stable derivatives and its reactivity in various chemical processes.

2847-91-8

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2847-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2847-91-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,4 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2847-91:
(6*2)+(5*8)+(4*4)+(3*7)+(2*9)+(1*1)=108
108 % 10 = 8
So 2847-91-8 is a valid CAS Registry Number.

2847-91-8SDS

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 DIETHYL 2-ACETAMIDO-2-(3-OXO-3-PHENYLPROPYL)MALONATE

1.2 Other means of identification

Product number -
Other names 2-Acetamino-2-aethoxycarbonyl-4-benzoyl-buttersaeure-aethylester

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:2847-91-8 SDS

2847-91-8Relevant academic research and scientific papers

Conformationally restricted analogs of histamine H1 receptor antagonists: trans and cis 1 benzyl 3 dimethylamino 6 phenylpiperidine

Ahmed,Hanna,Grund

, p. 117 - 122,118, 120 (1976)

The syntheses of trans and cis 1 benzyl 3 dimethylamino 6 phenylpiperidine (1 and 2) are described. Compounds 1 and 2 were found to be inhibitors of histamine, acetylcholine, and barium chloride induced contractions of the isolated guinea pig ileum. Compounds 1 and 2 do not exhibit appreciable stereoselectivity in their ability to inhibit smooth muscle contractions. The cis compound 2 is a more effective inhibitor of histamine N methyltransferase than the trans isomer 1.

Double diastereoselectivite de la cycloaddition dipolaire-1,3 d'ylures d'azomethine cycliques substitues

Lakhlifi, Tahar,Sedqui, Ahmed,Fathi, Toufik,Laude, Bernard,Robert, Jean-Francois

, p. 1417 - 1423 (2007/10/02)

Seven derivatives of methyl 5-phenyl-3,4-dihydro-2H-pyrrole-2-carboxylates 1 were synthesized.These compounds are precursors of pentagonal cyclic azomethine ylides, the two sides of which are diastereotopic.The 1,3-dipolar species react with N-methyl and

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