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[1,1'-Biphenyl]-4-amine, 2,4'-dichlorois a chemical compound with the chemical formula C12H8Cl2N. It belongs to the amine and biphenyl chemical classes and is characterized by the presence of a 2,4'-dichloro substituent on the biphenyl ring. [1,1'-Biphenyl]-4-amine, 2,4'-dichlorois commonly used in organic synthesis and pharmaceutical research as a starting point for the synthesis of various biologically active compounds. Its chemical structure and properties make it valuable for the development of new drugs, pesticides, and other chemical products. Additionally, it also has potential applications in the field of materials science, as it can be incorporated into various polymers and materials to impart specific properties or functions.

138588-57-5

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138588-57-5 Usage

Uses

Used in Pharmaceutical Research:
[1,1'-Biphenyl]-4-amine, 2,4'-dichlorois used as a starting material for the synthesis of biologically active compounds in pharmaceutical research. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, [1,1'-Biphenyl]-4-amine, 2,4'-dichlorois used as a building block for creating more complex molecules. Its reactivity and functional groups make it a versatile component in the synthesis of various organic compounds.
Used in Pesticide Development:
[1,1'-Biphenyl]-4-amine, 2,4'-dichlorois used as a chemical intermediate in the development of new pesticides. Its properties can be exploited to create effective and targeted pest control agents.
Used in Materials Science:
In the field of materials science, [1,1'-Biphenyl]-4-amine, 2,4'-dichlorois used for incorporating specific properties or functions into polymers and other materials. Its chemical structure can enhance the performance of these materials in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 138588-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,8 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138588-57:
(8*1)+(7*3)+(6*8)+(5*5)+(4*8)+(3*8)+(2*5)+(1*7)=175
175 % 10 = 5
So 138588-57-5 is a valid CAS Registry Number.

138588-57-5SDS

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 3 -chloro-4-(4-chlorophenyl)benzenamine

1.2 Other means of identification

Product number -
Other names 3-chloro-4-(4-chlorophenyl)benzenamine

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:138588-57-5 SDS

138588-57-5Relevant academic research and scientific papers

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

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Paragraph 00488; 00489; 001123; 001124, (2021/01/22)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with a defect in glyoxylate metabolism, for example a disease or disorder associated with the enzyme glycolate oxidase (GO) or alterations in oxalate metabolism. Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

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Paragraph 00530; 00531; 00532; 001165; 001166; 001167, (2019/07/17)

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme glycolate oxidase (GO). Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

COMBINATION THERAPIES FOR TREATMENT OF CANCER

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Page/Page column 252, (2016/04/09)

Combination therapies for treatment of cancers associated with mutations in the KRAS gene are provided. Compositions comprising therapeutic agents for treatment of cancers associated with mutations in the KRAS gene are also provided.

INHIBITORS OF KRAS G12C

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Page/Page column 199; 200, (2015/04/28)

Compounds having activity as inhibitors of G12C mutant KRAS protein are provided. The compounds have the following structure (I): or a pharmaceutically acceptable salt, tautomer, prodrug or stereoisomer thereof, wherein R1, R2a, R3a, R3b, R4a, R4b, G1, G2, L1, L2, m1, m2, A, B, W, X, Y, Z and E are as defined herein. Methods associated with preparation and use of such compounds, pharmaceutical compositions comprising such compounds and methods to modulate the activity of G12C mutant KRAS protein for treatment of disorders, such as cancer, are also provided.

BIPHENYL DERIVATIVES USEFUL AS GLUCAGON RECEPTOR ANTAGONISTS

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Page/Page column 29, (2012/12/13)

The present invention is directed to biphenyl derivatives, pharmaceutical compositions containing them and their use in the treatment and/or prevention of disorders and conditions ameliorated by antagonizing one or more glucagon receptors, including for example metabolic diseases such as Type II diabetes mellitus and obesity.

PICOLINAMIDO-PROPANOIC ACID DERIVATIVES USEFUL AS GLUCAGON RECEPTOR ANTAGONISTS

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Page/Page column 29, (2012/12/13)

The present invention is directed to picolanmido-propanoic acid derivatives, pharmaceutical compositions containing them and their use in the treatment and/or prevention of disorders and conditions ameliorated by antagonizing one or more glucagon receptors, including for example metabolic diseases such as Type II diabetes mellitus and obesity.

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