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57079-16-0

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57079-16-0 Usage

Description

N-(10-CARBOXYDECANYL)MALEAMIDEIC ACID, with the CAS number 57079-16-0, is a white solid compound that is primarily utilized in the field of organic synthesis. Its chemical structure and properties make it a valuable component in the creation of various organic compounds and materials.

Uses

Used in Organic Synthesis:
N-(10-CARBOXYDECANYL)MALEAMIDEIC ACID is used as a synthetic building block for the development of new organic compounds. Its unique structure allows it to be a key component in the synthesis of various molecules, contributing to the advancement of organic chemistry and the creation of novel materials.
Used in Pharmaceutical Industry:
N-(10-CARBOXYDECANYL)MALEAMIDEIC ACID is used as an intermediate in the synthesis of pharmaceutical compounds. Its chemical properties make it suitable for the development of new drugs, potentially leading to the discovery of innovative treatments for various medical conditions.
Used in Chemical Research:
N-(10-CARBOXYDECANYL)MALEAMIDEIC ACID is used as a research tool in the field of chemistry. Its unique properties and reactivity enable scientists to study its interactions with other molecules, leading to a better understanding of chemical reactions and the development of new synthetic methods.
Used in Material Science:
N-(10-CARBOXYDECANYL)MALEAMIDEIC ACID is used as a component in the development of new materials. Its chemical structure can be manipulated to create materials with specific properties, such as improved strength, flexibility, or chemical resistance, which can be applied in various industries, including electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 57079-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,7 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57079-16:
(7*5)+(6*7)+(5*0)+(4*7)+(3*9)+(2*1)+(1*6)=140
140 % 10 = 0
So 57079-16-0 is a valid CAS Registry Number.

57079-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(10-Carboxydecanyl)maleamideic Acid

1.2 Other means of identification

Product number -
Other names 11-{[(2Z)-3-Carboxy-2-propenoyl]amino}undecanoic acid

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:57079-16-0 SDS

57079-16-0Relevant articles and documents

Thermally reversible crosslinked polyethylene using Diels-Alder reaction in molten state

Magana, Sylvain,Zerroukhi, Amar,Jegat, Corinne,Mignard, Nathalie

experimental part, p. 442 - 448 (2011/12/16)

Thermally reversible crosslinked polyethylene was prepared by Diels-Alder (DA) and retro Diels-Alder (rDA) reaction. Maleimide/furan adduct was used as crosslinking agent. Dienophile named 11-maleimido-undecanoic acid was first synthesized and between this dienophile and commercial 3-(2-furyl) propanoic acid, the DA reaction was studied to determine DA and rDA reactions temperatures in the solid state. Then, an original modification method was employed to graft the two molecules onto the Lotader poly(ethylene-co-glycidyl methacrylate) in one step procedure. The DA and rDA reactions between diene and dienophile grafted moieties are followed by FT-IR analysis on a thin film. Readily polymer network is synthesized and the cycle of DA and retro-DA reactions is repeatable with no significant polymer degradation.

Alkylating derivatives of amino acids and peptides. Synthesis of N-maleoylamino acids, [1-(N-maleoylglycyl)cysteinyl]oxytocin, and [1-(N-maleoyl-11-aminoundecanoyl)cysteinyl]oxytocin. Effects on vasopressin-stimulated water loss from isolated toad bladder.

Rich,D.H. et al.

, p. 1004 - 1010 (2007/10/11)

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