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17675-42-2

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17675-42-2 Usage

General Description

4-AMINO-N-CYCLOHEXYLBENZAMIDE is a chemical compound with the molecular formula C13H17N3O and a molecular weight of 231.29 g/mol. It is a benzamide derivative with a cyclohexylamine moiety and an amino group. 4-AMINO-N-CYCLOHEXYLBENZAMIDE has been studied for its potential applications in pharmaceuticals and agrochemicals, as well as in the development of organic dyes and pigments. It is also used as a building block in chemical synthesis. 4-AMINO-N-CYCLOHEXYLBENZAMIDE may have potential biological activities and may be used as a precursor for the preparation of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 17675-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,7 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17675-42:
(7*1)+(6*7)+(5*6)+(4*7)+(3*5)+(2*4)+(1*2)=132
132 % 10 = 2
So 17675-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O/c14-11-8-6-10(7-9-11)13(16)15-12-4-2-1-3-5-12/h6-9,12H,1-5,14H2,(H,15,16)

17675-42-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-N-cyclohexylbenzamide

1.2 Other means of identification

Product number -
Other names 4-Amino-N-cyclohexyl-benzamid

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:17675-42-2 SDS

17675-42-2Relevant articles and documents

Discovery of memantyl urea derivatives as potent soluble epoxide hydrolase inhibitors against lipopolysaccharide-induced sepsis

Bao, Xuefei,Chen, Guoliang,Du, Fangyu,Hammock, Bruce D.,Liu, Qiu,Liu, Zhongbo,Morisseau, Christophe,Sun, Wenjiao,Wang, Chao,Xiao, Wei,Yang, Hao,Zhang, Tan,Zhou, Jun

, (2021)

Sepsis, a systemic inflammatory response, caused by pathogenic factors including microorganisms, has high mortality and limited therapeutic approaches. Herein, a new soluble epoxide hydrolase (sEH) inhibitor series comprising a phenyl ring connected to a

sEH inhibitor and preparation method and application thereof

-

Paragraph 0234; 0236; 0239-0240, (2020/07/28)

The invention provides an sEH inhibitor and a preparation method and application thereof, and relates to the technical field of endogenous active substance regulation and control. The sEH inhibitor provided by the invention has a structure as shown in a f

PURINE AND 3-DEAZAPURINE ANALOGUES AS CHOLINE KINASE INHIBITORS

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Page/Page column 119, (2018/02/28)

There are provided substituted purine and 3-deazapurine analogues, which modulate the activity of Choline Kinase (ChoK). The compounds of this invention are therefore useful in treating diseases caused by an altered choline metabolism, such as cancer, cell proliferative disorders, infectious diseases of different origin, immune-related disorders and neurodegenerative disorders. The present invention also provides methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and methods of treating diseases utilizing pharmaceutical compositions comprising these compounds.

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