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2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid is a complex organic compound characterized by its molecular structure that features two benzene rings connected by a carbon chain. 2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid is notable for its multiple amine and carbonyl functional groups, which suggest a high degree of reactivity and the potential for interactions with biological systems. The presence of long-chain alkyl groups hints at surfactant properties and possible involvement in lipid interactions. As a carboxylic acid derivative, it possesses acidic characteristics and the capacity to form salts with other compounds. The diverse chemical features of 2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid make it a potentially versatile and impactful molecule in fields such as pharmaceuticals, materials science, and biological research.

2352-88-7

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2352-88-7 Usage

Uses

Used in Pharmaceutical Industry:
2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid is used as a pharmaceutical agent for its potential reactivity and interactions with biological systems. 2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid's amine and carbonyl groups may allow it to form complexes with biological molecules, making it a candidate for drug development, particularly in targeting specific receptors or enzymes.
Used in Materials Science:
In the field of materials science, 2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid is used as a component in the development of new materials. Its surfactant properties and ability to interact with lipids could be leveraged in the creation of advanced materials with specific surface properties or for use in drug delivery systems.
Used in Biological Research:
2-[[bis[2-[(1-oxooctadecyl)amino]ethyl]amino]carbonyl]benzoic acid is utilized as a research tool in biological studies. Its complex structure and functional groups make it a valuable probe for understanding the interactions between small molecules and biological systems, potentially leading to insights into new mechanisms of action or the discovery of novel bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 2352-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2352-88:
(6*2)+(5*3)+(4*5)+(3*2)+(2*8)+(1*8)=77
77 % 10 = 7
So 2352-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C48H85N3O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-37-45(52)49-39-41-51(47(54)43-35-33-34-36-44(43)48(55)56)42-40-50-46(53)38-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h33-36H,3-32,37-42H2,1-2H3,(H,49,52)(H,50,53)(H,55,56)

2352-88-7SDS

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 2-[bis[2-(octadecanoylamino)ethyl]carbamoyl]benzoic acid

1.2 Other means of identification

Product number -
Other names EINECS 219-088-9

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:2352-88-7 SDS

2352-88-7Upstream product

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