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3-(7-chloro-1-oxoisoindolin-2-yl)benzoic acid, with the chemical formula C16H10ClNO3, is an organic compound that belongs to the class of benzoic acids and derivatives. It is characterized by a carboxyl group (-COOH) attached to a benzene ring and has a molecular weight of 301.7 g/mol. This chemical compound is known for its high melting point and is typically white-to-off-white in color when in its solid-state. The presence of a chlorine atom in its structure contributes to its reactive properties, making it a versatile compound for various applications. Like most organic compounds, it is non-soluble in water but readily dissolves in organic solvents such as alcohol and acetone. However, it can be hazardous if not handled properly.

1044921-12-1

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1044921-12-1 Usage

Uses

Used in Pharmaceutical Industry:
3-(7-chloro-1-oxoisoindolin-2-yl)benzoic acid is used as an active pharmaceutical ingredient for the development of various medications. Its unique chemical structure allows it to interact with biological targets, making it a promising candidate for the treatment of different diseases and medical conditions.
Used in Plastics Industry:
In the plastics industry, 3-(7-chloro-1-oxoisoindolin-2-yl)benzoic acid is used as a monomer or a building block for the synthesis of various polymers. Its reactive properties enable it to form covalent bonds with other monomers, resulting in the creation of new polymers with specific properties, such as improved strength, flexibility, or heat resistance.
Used in Chemical Industry:
3-(7-chloro-1-oxoisoindolin-2-yl)benzoic acid is utilized as a key intermediate in the synthesis of various chemical compounds and materials. Its reactive chlorine atom allows it to participate in various chemical reactions, such as substitution, addition, or elimination reactions, leading to the formation of new compounds with diverse applications in the chemical industry.
Used in Organic Synthesis:
3-(7-chloro-1-oxoisoindolin-2-yl)benzoic acid serves as a valuable starting material for organic synthesis, where it can be further modified or functionalized to produce a wide range of organic compounds. Its unique structure and reactivity make it suitable for the synthesis of various pharmaceuticals, agrochemicals, dyes, and other specialty chemicals.
Used in Research and Development:
In the field of research and development, 3-(7-chloro-1-oxoisoindolin-2-yl)benzoic acid is employed as a model compound to study various chemical reactions and mechanisms. Its unique structure and reactivity provide insights into the behavior of similar compounds and contribute to the advancement of organic chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1044921-12-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,9,2 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1044921-12:
(9*1)+(8*0)+(7*4)+(6*4)+(5*9)+(4*2)+(3*1)+(2*1)+(1*2)=121
121 % 10 = 1
So 1044921-12-1 is a valid CAS Registry Number.

1044921-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chloro-3-oxo-1H-isoindol-2-yl)benzoic acid

1.2 Other means of identification

Product number -
Other names 3-(7-chloro-1-oxoisoindolin-2-yl)benzoic 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:1044921-12-1 SDS

1044921-12-1Upstream product

1044921-12-1Downstream Products

1044921-12-1Relevant articles and documents

Pharmacological, pharmacokinetic, and primate analgesic efficacy profile of the novel bradykinin B1 receptor antagonist ELN441958

Hawkinson, Jon E.,Szoke, Balazs G.,Garofalo, Albert W.,Hom, Dennis S.,Zhang, Hongbing,Dreyer, Mark,Fukuda, Juri Y.,Chen, Linda,Samant, Bhushan,Simmonds, Stellanie,Zeitz, Karla P.,Wadsworth, Angie,Liao, Anna,Chavez, Raymond A.,Zmolek, Wes,Ruslim, Lany,Bova, Michael P.,Holcomb, Ryan,Butelman, Eduardo R.,Ko, Mei-Chuan,Malmberg, Annika B.

, p. 619 - 630 (2007)

The bradykinin B1 receptor plays a critical role in chronic pain and inflammation, although efforts to demonstrate efficacy of receptor antagonists have been hampered by species-dependent potency differences, metabolic instability, and low oral

Novel compounds useful for bradykinin B1 receptor antagonism

-

Page/Page column 32, (2010/11/25)

Disclosed are compounds that are bradykinin B1 receptor antagonists and are useful for treating diseases, or relieving adverse symptoms associated with disease conditions, in mammals mediated by bradykinin B1 receptor.

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