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105699-82-9

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105699-82-9 Usage

General Description

1,3-Benzenedicarboxylic acid, 5,5'-(carbonyldiimino)bis- is a chemical compound commonly known as a phthalimide derivative. It is used in various industrial applications, including as a building block in the synthesis of polymers, dyes, and pharmaceuticals. 1,3-Benzenedicarboxylic acid, 5,5'-(carbonyldiimino)bis- is a white solid with a high melting point, and it is soluble in various organic solvents. It is an important intermediate in the production of polyimides, which are high-performance engineering plastics known for their thermal stability and mechanical strength. Additionally, it has been studied for potential use in drug delivery systems and as an antioxidant in various materials.

Check Digit Verification of cas no

The CAS Registry Mumber 105699-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,6,9 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 105699-82:
(8*1)+(7*0)+(6*5)+(5*6)+(4*9)+(3*9)+(2*8)+(1*2)=149
149 % 10 = 9
So 105699-82-9 is a valid CAS Registry Number.

105699-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5'-(carbonylbis(azanediyl))diisophthalic acid

1.2 Other means of identification

Product number -
Other names -

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:105699-82-9 SDS

105699-82-9Downstream Products

105699-82-9Relevant articles and documents

Urea metal-organic frameworks as effective and size-selective hydrogen-bond catalysts

Roberts, John M.,Fini, Branden M.,Sarjeant, Amy A.,Farha, Omar K.,Hupp, Joseph T.,Scheidt, Karl A.

, p. 3334 - 3337 (2012/04/10)

A new urea-containing metal-organic framework (MOF) was synthesized to act as a heterogeneous catalyst. Ureas are well-known for self-recognition and aggregation behavior, resulting in loss of catalytic competency. The catalyst spatial isolation achievable in a porous MOF environment suggests a potentially general solution. The combination of a symmetrical urea tetracarboxylate strut, 4,4′-bipyridine, and Zn(NO3)2?6H2O under solvothermal conditions afforded a new microporous MOF (NU-601). This material is indeed an effective hydrogen-bond-donor catalyst for Friedel-Crafts reactions between pyrroles and nitroalkenes, whereas a homogeneous urea is much less competent. The higher rates of reaction of small substrates relative to larger ones with NU-601 strongly suggest that catalysis primarily occurs within the pores of this new material rather than on its exterior. To the best of our knowledge, this approach is the first example of specific engineering of successful hydrogen-bonding catalysis into a MOF material.

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