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DIETHYL 2-ANILINOMALONATE, with the molecular formula C17H19NO4, is a colorless to light yellow liquid characterized by a sweet, fruity odor. It is a versatile chemical compound that serves as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. Its ability to participate in various chemical reactions makes it an important building block in the production of fine chemicals and active pharmaceutical ingredients. Due to its potential hazards, it is crucial to handle DIETHYL 2-ANILINOMALONATE with care and follow safety guidelines to prevent harm from swallowing, inhalation, or skin contact.

6414-58-0

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6414-58-0 Usage

Uses

Used in Pharmaceutical Industry:
DIETHYL 2-ANILINOMALONATE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex organic molecules. Its versatility in chemical reactions contributes to the development of new drugs and medicinal compounds.
Used in Dye Industry:
In the dye industry, DIETHYL 2-ANILINOMALONATE is utilized as a precursor in the production of dyes, where its chemical properties allow for the formation of diverse colorants used in textiles, printing, and other applications.
Used in Organic Synthesis:
DIETHYL 2-ANILINOMALONATE is employed as a building block in organic synthesis, enabling the construction of a wide range of organic compounds. Its reactivity and compatibility with various chemical processes make it a valuable component in the synthesis of specialty chemicals and advanced materials.
Used in Fine Chemicals Production:
As a component in the production of fine chemicals, DIETHYL 2-ANILINOMALONATE contributes to the development of high-quality, specialized chemicals used in research, pharmaceuticals, and other industries. Its role in this context is to provide a foundation for the synthesis of complex and high-value chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 6414-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6414-58:
(6*6)+(5*4)+(4*1)+(3*4)+(2*5)+(1*8)=90
90 % 10 = 0
So 6414-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO4/c1-3-17-12(15)11(13(16)18-4-2)14-10-8-6-5-7-9-10/h5-9,11,14H,3-4H2,1-2H3

6414-58-0SDS

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-anilinopropanedioate

1.2 Other means of identification

Product number -
Other names 2-Phenylamino-malonic 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:6414-58-0 SDS

6414-58-0Relevant academic research and scientific papers

Continuous-flow electro-oxidative coupling of sulfides with activated methylene compounds leading to sulfur ylides

Cai, Chen,Fang, Zheng,Guo, Kai,Lin, Yang,Liu, Chengkou,Yuan, Chengcheng

, p. 2956 - 2961 (2021/05/05)

An unprecedentedly straightforward electro-oxidative coupling of sulfides with activated methylene compounds to synthesize sulfur ylides has been developed. Good to excellent yields can be obtained under catalyst- and oxidant-free conditions at room tempe

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

Thiazolo[3,2-a]pyrimidines, derivatives thereof, processes for production thereof, and pharmaceutical use thereof

-

, (2008/06/13)

A compound selected from thiazolo[3,2-a]pyrimidines or their enolate derivatives represented by the following general formula STR1 wherein R1 and R2 are identical or different, and each represents a hydrogen atom, an alkyl group havi

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