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Diethyl (acetylamino)(3-nitrobenzyl)propanedioate is a complex organic compound with the chemical formula C18H22N2O8. It is a derivative of propanedioic acid, featuring an acetylamino group and a 3-nitrobenzyl group attached to the central propanedioate backbone. diethyl (acetylamino)(3-nitrobenzyl)propanedioate is characterized by its ester linkages with two ethyl groups and a nitro group on the benzene ring, which contributes to its reactivity and potential applications in chemical synthesis. It is likely to be used in the preparation of pharmaceuticals or other specialty chemicals due to its structural complexity and functional groups.

5432-19-9

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5432-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5432-19-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5432-19:
(6*5)+(5*4)+(4*3)+(3*2)+(2*1)+(1*9)=79
79 % 10 = 9
So 5432-19-9 is a valid CAS Registry Number.

5432-19-9SDS

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 m-Toluidino-malonsaeure-diaethylester

1.2 Other means of identification

Product number -
Other names diethyl 3-methylphenylaminomalonate

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:5432-19-9 SDS

5432-19-9Relevant academic research and scientific papers

Ribosomal Synthesis of Macrocyclic Peptides in Vitro and in Vivo Mediated by Genetically Encoded Aminothiol Unnatural Amino Acids

Frost, John R.,Jacob, Nicholas T.,Papa, Louis J.,Owens, Andrew E.,Fasan, Rudi

, p. 1805 - 1816 (2015/09/01)

A versatile method for orchestrating the formation of side chain-to-tail cyclic peptides from ribosomally derived polypeptide precursors is reported. Upon ribosomal incorporation into intein-containing precursor proteins, designer unnatural amino acids be

MACROCYCLIC PEPTIDOMIMETICS FOR ALPHA-HELIX MIMICRY

-

Paragraph 00255, (2015/11/02)

Methods and compositions are provided for generating macrocyclic peptides constrained by side-chain-to-C-terminus non-peptidic tethers for use as functional and structural mimics of α-helical motifs, including in therapeutic applications. These methods can be used to produce libraries of conformationally constrained peptidomimetics to identify compounds with desired activity properties.

Use of 2-aminothiazoline derivatives as inhibitors of inducible no-synthase

-

, (2008/06/13)

The present invention relates to the use of 2-aminothiazoline derivatives of formula: in which either R1 is a hydrogen atom or an alkyl radical and R2 is an alkyl, -alk-NH2, —CH2—R3, —CH2—S

Streptogramins for preparing same by mutasynthesis

-

, (2008/06/13)

The invention provides a method for preparing streptogramins using genetically-modified microorganisms to influence the biosynthesis of at least one of the precursors of the group B streptogramins. Cultures of the genetically-modified microorganisms are supplemented with a least one precursor that is different from the streptogramin precursor whose biosynthesis is altered and the streptogramins produced are recovered.

Gonadotropin-Releasing Hormone Antagonists: Novel Members of the Azaline B Family

Rivier, Jean E.,Jiang, Guangcheng,Porter, John,Hoeger, Carl A.,Craig, A. Grey,et al.

, p. 2649 - 2662 (2007/10/03)

A series of antagonists of gonadotropin-releasing hormone (GnRH) homologous to azaline B (1, DCpa2, DPal3, Aph5(Atz), DAph6(Atz), ILys8, DAla10>GnRH) was synthesized, cha

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