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1,3-Benzenedicarboxamide, N,N'-dimethyl-, also known as N,N'-dimethyl isophthalamide, is an organic compound with the chemical formula C10H12N2O4. It is a white crystalline solid that is soluble in water and various organic solvents. 1,3-BenzenedicarboxaMide, N,N'-diMethyl- is derived from isophthalic acid, where two methyl groups are attached to the amine groups of the isophthalamide structure. It is primarily used as a monomer in the production of high-performance polymers, such as polyamides and polyimides, which are known for their excellent thermal stability, mechanical properties, and chemical resistance. These polymers find applications in various industries, including automotive, electronics, and aerospace.

6780-97-8

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6780-97-8 Usage

Use

Crosslinking agent in polyurethane-based materials and other industrial processes

Physical State

White crystalline powder

Solubility

Soluble in organic solvents

Melting Point

High

Properties

Enhances mechanical and thermal properties of polymers

Applications

Production of plastic and rubber products, adhesives, coatings, and sealants

Durability

Improves durability and strength of materials

Safety

Toxic if ingested or inhaled, may cause skin and eye irritation

Handling

Handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 6780-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6780-97:
(6*6)+(5*7)+(4*8)+(3*0)+(2*9)+(1*7)=128
128 % 10 = 8
So 6780-97-8 is a valid CAS Registry Number.

6780-97-8SDS

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 N,N'-bis-methylisophthaldiamide

1.2 Other means of identification

Product number -
Other names Isophthalsaeure-bis-methlylamid

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:6780-97-8 SDS

6780-97-8Downstream Products

6780-97-8Relevant academic research and scientific papers

Tandem Transformation of Aldoximes to N-Methylated Amides Using Methanol

Paul, Bhaskar,Maji, Milan,Panja, Dibyajyoti,Kundu, Sabuj

supporting information, p. 5357 - 5362 (2019/11/14)

Tandem conversion of aldoximes to N-methylated amides with methanol in presence of a single Ru(II) catalyst is accomplished through the Ru(II)-mediated rearrangement followed by the reductive N-methylation. Employing this protocol, several aldoximes were directly transformed to the N-methylated amides using methanol. Kinetic experiments with H218O advocated that the aldoxime is acted as the nucleophile during the aldoxime to amide rearrangement process. Involvement of nitrile intermediate during this transformation is realized from the kinetic study. (Figure presented.).

A supramolecular system for quantifying aromatic stacking interactions

Adams, Harry,Hunter, Christopher A.,Lawson, Kevin R.,Perkins, Julie,Spey, Sharon E.,Urch, Christopher J.,Sanderson, John M.

, p. 4863 - 4877 (2007/10/03)

A supramolecular complex for investigating the thermodynamic properties of intermolecular aromatic stacking interactions has been developed. The conformation of the complex is locked in a single well-defined conformation by an array of H-bonding interacti

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