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Dimethyl 3-aminopent-2-enedioate, also known as dimethyl 2-amino-3-methyl-2-butenedioate, is a chemical compound with the molecular formula C7H11NO4. It is a derivative of malic acid and is commonly used as a chelating agent in the food and pharmaceutical industries. dimethyl 3-aminopent-2-enedioate is also utilized in the synthesis of various pharmaceutical drugs and organic compounds due to its ability to form stable complexes with metal ions. Additionally, dimethyl 3-aminopent-2-enedioate has applications in the field of chemistry research, particularly in the study of coordination chemistry and metal-ligand interactions. Overall, this chemical compound plays a crucial role in various industrial and scientific applications.

63547-62-6

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63547-62-6 Usage

Uses

Used in Food Industry:
Dimethyl 3-aminopent-2-enedioate is used as a chelating agent to bind metal ions, which helps to prevent oxidation and spoilage of food products, thereby extending their shelf life.
Used in Pharmaceutical Industry:
Dimethyl 3-aminopent-2-enedioate is used as a chelating agent in the formulation of pharmaceutical drugs, enhancing their stability and bioavailability.
Used in Chemical Research:
Dimethyl 3-aminopent-2-enedioate is used as a ligand in coordination chemistry, enabling the study of metal-ligand interactions and the development of new compounds with potential applications in various fields.
Used in Synthesis of Pharmaceutical Drugs:
Dimethyl 3-aminopent-2-enedioate is used as a key intermediate in the synthesis of various pharmaceutical drugs, contributing to the development of new medications with improved therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 63547-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63547-62:
(7*6)+(6*3)+(5*5)+(4*4)+(3*7)+(2*6)+(1*2)=136
136 % 10 = 6
So 63547-62-6 is a valid CAS Registry Number.

63547-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (E)-3-aminopent-2-enedioate

1.2 Other means of identification

Product number -
Other names dimethyl-3-enamino-glutarate

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:63547-62-6 SDS

63547-62-6Relevant academic research and scientific papers

Scalable non-aqueous process to prepare water soluble 3-amino-pentan-1,5- diol

Rawalpally, Thimma,Ji, Yaohui,Cleary, Thomas,Edwards, Billy

, p. 478 - 482 (2009)

The development of a nonaqueous process for the synthesis of 3-amino-pentan-1,5-diol is described. Beginning with dimethyl acetone-1,3-dicarboxylate, a telescoped sequence of reductive amination, Boc protection, sodium borohydride reduction, and acidic resin-mediated deprotection generates the title compound. The key to this efficient process is the telescoped deprotection, purification and nonaqueous isolation of the 3-amino-pentan-1,5- diol. The process involves four optimized chemical reactions using two solvents in 89% overall yield and 97-98 area % purity.

PYRIMIDINES AND VARIANTS THEREOF, AND USES THEREFOR

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Paragraph 00419; 00420, (2017/10/13)

The present disclosure provides pyrimidine compounds and uses thereof, for example, for the treatment of diseases associated with P2X purinergic receptors. In certain aspects, the present disclosure provides P2X3 and/or P2X2/3 antagonists which are useful, for example, for the treatment of visceral organ, cardiovascular and pain-related diseases, conditions and disorders.

NOVEL PROCESS FOR THE PREPARATION OF 3-AMINO-PENTAN-1,5-DIOL

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Page/Page column 3; 5, (2009/01/24)

The present invention provides a novel method for preparing a key intermediate, 3-amino-pentan-1,5-diol (2), which is useful for the preparation of 6-(2,4-difluorophenoxy)-2-[3-hydroxy-1-(2-hydroxyethyl)-propylamino]-8-methyl-8H-pyrido[2,3-d]pyrimidine-7-one (1) a MAP-kinase inhibitor useful in the treatment of rheumatoid arthritis.

PYRIDINE COMPOUNDS AS INHIBITORS OF DIPEPTIDYL PEPTIDASE IV

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Page/Page column 98, (2010/02/11)

A compound represented by the formula wherein R1 and R2 are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted hydroxy group; R3 is an optionally substituted aromatic group; R4 is an optionally substituted amino group; L is a divalent chain hydrocarbon group; Q is a bond or a divalent chain hydrocarbon group; and X is a hydrogen atom, a cyano group, a nitro group, an acyl group, a substituted hydroxy group, an optionally substituted thiol group, an optionally substituted amino group or an optionally substituted cyclic group; provided that when X is an ethoxycarbonyl group, then Q is a divalent chain hydrocarbon group. The compound has a peptidase inhibitory action, is useful as an agent for the prophylaxis or treatment of diabetes and the like, and is superior in efficacy, duration of action, specificity, lower toxicity and the like.

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