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106037-36-9

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106037-36-9 Usage

Description

Benzamide, 4-amino-3-methyl(9CI), also known as 4-amino-3-methylbenzamide, is an organic compound with the molecular formula C8H10N2O. It belongs to the group of compounds known as benzoic acid and derivatives, which are characterized by a benzene ring bearing at least one carboxylic acid substituent. Benzamide, 4-amino-3-methyl(9CI) can exist in various physical forms and is commonly utilized in chemical research and manufacturing. As with many other chemicals, the specific properties, potential applications, and associated health risks of Benzamide, 4-amino-3-methyl(9CI) would necessitate further detailed study and investigation.

Uses

Used in Chemical Research:
Benzamide, 4-amino-3-methyl(9CI) is used as a research compound for the development and synthesis of new chemical entities. Its unique structure allows for exploration in various chemical reactions and the potential discovery of novel applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Benzamide, 4-amino-3-methyl(9CI) is used as an intermediate in the synthesis of various drugs. Its presence in the molecular structure of certain compounds can contribute to their therapeutic properties, making it a valuable component in drug development.
Used in Material Science:
Benzamide, 4-amino-3-methyl(9CI) is employed as a building block in the creation of new materials with specific properties. Its chemical structure can be manipulated to achieve desired characteristics, such as improved stability or enhanced reactivity, in the final material.
Used in Analytical Chemistry:
As an analytical reagent, Benzamide, 4-amino-3-methyl(9CI) is used for the identification and quantification of various substances in complex mixtures. Its unique chemical properties can be exploited to develop sensitive and selective analytical methods for detecting target compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 106037-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,3 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 106037-36:
(8*1)+(7*0)+(6*6)+(5*0)+(4*3)+(3*7)+(2*3)+(1*6)=89
89 % 10 = 9
So 106037-36-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O/c1-5-4-6(8(10)11)2-3-7(5)9/h2-4H,9H2,1H3,(H2,10,11)

106037-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-3-methylbenzamide

1.2 Other means of identification

Product number -
Other names 4-aMino-3-MethylbenzaMide

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:106037-36-9 SDS

106037-36-9Relevant articles and documents

Non-nucleoside reverse transcriptase inhibitors

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Page/Page column 23, (2008/06/13)

The present invention provides for compounds useful for treating an HIV-1 infection, or preventing an HIV-1 infection, or treating AIDS or ARC. The compounds of the invention are of formula I wherein R1, R2, R3, R4, R5 and X are as herein defined. Also disclosed in the present invention are methods of treating an HIV infection with compounds defined herein and pharmaceutical compositions containing said compounds. [image]

Substituted 1-phenyl-3-pyrazolecarboxamides active on neurotensin receptors, their preparation and pharmaceutical compositions containing them

-

, (2008/06/13)

The invention relates to new substituted 1-phenyl-3-pyrazolecarboxamides having a great affinity for human neurotensin receptors, to a process for preparing them and to pharmaceutical compositions containing them as active principles. More particularly, this invention relates to the discovery that the affinity for neurotensin receptors, especially human neurotensin receptors, is increased by substituting the phenyl group of 1-phenyl-3-pyrazolecarboxamide compounds with particular groups.

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