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Diethyl [(4-methylphenyl)amino]propanedioate is a chemical compound with the molecular formula C14H19NO4. It is an organic ester derived from the combination of 4-methylaniline and diethyl propanedioate. diethyl [(4-methylphenyl)amino]propanedioate is characterized by its aromatic 4-methylphenyl group attached to an aminopropanedioate moiety, which is esterified with two ethyl groups. It is a colorless to pale yellow liquid with a mild, characteristic odor. Diethyl [(4-methylphenyl)amino]propanedioate is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows it to participate in a range of chemical reactions, making it a versatile building block in organic synthesis.

5634-67-3

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5634-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5634-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5634-67:
(6*5)+(5*6)+(4*3)+(3*4)+(2*6)+(1*7)=103
103 % 10 = 3
So 5634-67-3 is a valid CAS Registry Number.

5634-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-(4-methylanilino)propanedioate

1.2 Other means of identification

Product number -
Other names <4-Toluidino>-malonsaeure-diethylester

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:5634-67-3 SDS

5634-67-3Relevant academic research and scientific papers

Iridium catalyzed acceptor/acceptor carbene insertion into N-H bonds in water

Ramakrishna, Kankanala,Sivasankar, Chinnappan

supporting information, p. 2392 - 2396 (2017/03/20)

The chemistry of A and D/A carbenes (D and A are donor and acceptor groups, respectively) is known to a great extent in the literature. Nevertheless the chemistry of the A/A class of carbenes is less explored, although the A/A class of carbenes is more im

A convenient synthesis of 3-phenylthio-azetidin-2-ones

Bari,Sharma,Sethi

, p. 1114 - 1119 (2007/10/03)

3-Phenylthio-4,4-diethoxycarbonyl-azetidin-2-ones 8 have been conveniently synthesised by reacting 2-chlorophenylthioacetyl chloride 5 with aryl substituted aminomalonates 7 under mild basic conditions. Alternatively, C-3 alkylation of azetidin-2-one usin

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