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70693-59-3

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70693-59-3 Usage

Description

2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide, also known as 2-(cyclohexylmethylsulfamoyl)aniline, is a gray-white crystalline compound with unique chemical properties. It is characterized by the presence of an amino group, a cyclohexylmethylsulfamoyl group, and a benzene ring, which contribute to its potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide is used as an active pharmaceutical ingredient for the development of drugs targeting specific medical conditions. Its unique chemical structure allows it to interact with biological targets, making it a promising candidate for the treatment of various diseases.
Used in Chemical Synthesis:
In the field of organic chemistry, 2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide serves as a key intermediate in the synthesis of various complex organic compounds. Its versatile structure enables it to be modified and incorporated into a wide range of molecules, facilitating the development of new chemical entities with potential applications in various industries.
Used in Material Science:
2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide is utilized as a building block in the development of novel materials with specific properties. Its ability to form stable interactions with other molecules allows it to be incorporated into polymers, coatings, and other materials, enhancing their performance and expanding their potential applications.
Used in Research and Development:
As a unique chemical entity, 2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide is employed in research and development efforts to explore its potential applications and properties. Scientists and researchers use this compound to investigate its interactions with biological systems, its reactivity in chemical reactions, and its potential use in the development of new technologies and products.

Check Digit Verification of cas no

The CAS Registry Mumber 70693-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,9 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70693-59:
(7*7)+(6*0)+(5*6)+(4*9)+(3*3)+(2*5)+(1*9)=143
143 % 10 = 3
So 70693-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2O2S/c1-15(11-7-3-2-4-8-11)18(16,17)13-10-6-5-9-12(13)14/h5-6,9-11H,2-4,7-8,14H2,1H3

70693-59-3 Well-known Company Product Price

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  • Aldrich

  • (522325)  2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide  97%

  • 70693-59-3

  • 522325-25G

  • 1,387.62CNY

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70693-59-3SDS

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 2-Amino-N-cyclohexyl-N-methylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-AMINO-BENZENE-SULFON-N-METHYL CYCLOHEXYLAMIDE

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:70693-59-3 SDS

70693-59-3Downstream Products

70693-59-3Relevant articles and documents

Process for the catalytic hydrogeneration of aromatic nitro compounds

-

, (2008/06/13)

PCT No. PCT/EP96/01889 Sec. 371 Date Nov. 13, 1997 Sec. 102(e) Date Nov. 13, 1997 PCT Filed May 7, 1996 PCT Pub. No. WO96/36597 PCT Pub. Date Nov. 21, 1996One object of the invention is a process for the catalytic hydrogenation of aromatic nitro compounds in solution or in melt in the presence of hydrogen and at least one noble metal catalyst, nickel catalyst or cobalt catalyst, in which process a catalytic amount of at least one vanadium compound is present, wherein the vanadium has the oxidation state 0, II, IV or V. It has been found that in the catalytic hydrogenation of aromatic nitro compounds the accumulation of hydroxylamines can be almost completely prevented by the addition of catalytic amounts of vanadium compounds, which usually results in concentrations of 1% hydroxylamine. The resulting hydrogenated products are whiter (purer) than those obtained without the addition of the vanadium compound because almost no azo or azoxy compounds are obtained. The hydrogenation, in particular the final phase, proceeds faster than without said addition. Accordingly, substantial advantages with respect to quality constancy and economy are obtained.

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