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194805-15-7

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194805-15-7 Usage

Description

5-Bromo-2,3-dimethyl-phenylamine, also known as 5-BroMo-2,3-diMethyl-phenylaMine, is an aromatic amine with the chemical formula C8H10BrN. It features a bromine atom and two methyl groups attached to the phenyl ring, which endows it with unique chemical properties. 5-BroMo-2,3-diMethyl-phenylaMine serves as a versatile building block in various chemical and pharmaceutical applications.

Uses

Used in Organic Synthesis:
5-Bromo-2,3-dimethyl-phenylamine is used as a building block in organic synthesis for the creation of complex organic molecules. Its presence of bromine and methyl groups allows for a range of chemical reactions, facilitating the synthesis of diverse organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Bromo-2,3-dimethyl-phenylamine is utilized as a key component in the development of new drugs. Its unique structure and reactivity make it a valuable precursor in the synthesis of pharmaceutical intermediates, contributing to the discovery of novel therapeutic agents.
Used in the Preparation of Pharmaceutical Intermediates:
5-Bromo-2,3-dimethyl-phenylamine is used as a reagent in the preparation of pharmaceutical intermediates. Its chemical properties enable it to participate in various reactions, leading to the formation of intermediates that are crucial for the production of final drug products.
Used in Agrochemicals:
5-BroMo-2,3-diMethyl-phenylaMine also finds application in the agrochemical sector, where it is used in the synthesis of agrochemicals. Its role in the preparation of intermediates for agrochemicals aids in the development of effective products for agricultural use.
Used in the Manufacturing of Chemical Products:
5-Bromo-2,3-dimethyl-phenylamine is important in the manufacturing of various chemical products due to its chemical versatility. Its ability to participate in a wide array of chemical reactions makes it a valuable component in the production of different types of chemicals.
Used in Drug Development:
In the realm of drug development, 5-Bromo-2,3-dimethyl-phenylamine plays a significant role. Its unique structure and reactivity are harnessed in the synthesis of new drug candidates, contributing to the advancement of pharmaceutical science and the creation of innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 194805-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,8,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 194805-15:
(8*1)+(7*9)+(6*4)+(5*8)+(4*0)+(3*5)+(2*1)+(1*5)=157
157 % 10 = 7
So 194805-15-7 is a valid CAS Registry Number.

194805-15-7Relevant articles and documents

COMPOSITIONS FOR USE IN METHODS OF INHIBITING PROTEIN KINASES

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Paragraph 0016; 0086; 0087; 0104; 0105, (2018/10/25)

Identified compounds demonstrate protein kinase inhibitory activity and inhibition of dependent cell signaling pathways, such as NOD2 cell signaling. More specifically, the compounds are demonstrated to inhibit receptor interacting kinase 2 (RIPK2) and/or Activin- like kinase 2 (ALK2). Compounds that are either dual RIPK2/ALK2 inhibitors or that preferentially inhibit RIPK2 or ALK2 could provide therapeutic benefit.

4-Oxoquinolizine antimicrobial having 2-pyridone skeleton as partial structure

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, (2008/06/13)

A compound represented by the following Formula (I) or a pharmaceutically acceptable salt thereof: 1wherein R1 represents a hydrogen atom or a carboxyl-protecting group, R2 represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group or a hydroxyl group, R3 represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkylthio group, a nitro group, a cyano group, a hydroxyl group or an amino group; R4 represents a hydrogen atom, an amino-protecting group, an alkyl group or a cycloalkyl group, and R5 represents a hydrogen atom, a halogen atom, an alkyl group, an alkenyl group, a cycloalkyl group, an aryl group, an alkoxy group, an alkylthio group, a hydroxyl group, an imino group or an amino group.

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