36034-62-5 Usage
Uses
Used in Pharmaceutical Applications:
3-(3,5-DIMETHYL-PHENYLAMINO)-PROPIONITRILE is used as a chemical intermediate for the synthesis of various organic compounds, playing a crucial role in the development of new drugs or medications. Its potential therapeutic properties make it a promising candidate for pharmaceutical research and development.
Used in Research Applications:
In the field of organic chemistry, 3-(3,5-DIMETHYL-PHENYLAMINO)-PROPIONITRILE is used as a subject of study for its unique chemical structure and properties. It serves as an interesting target for researchers looking to understand and innovate within the realm of drug discovery and organic synthesis.
Used in Chemical Synthesis Industry:
3-(3,5-DIMETHYL-PHENYLAMINO)-PROPIONITRILE is used as a key component in the synthesis of complex organic molecules, contributing to the advancement of chemical processes and the creation of novel compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 36034-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,3 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36034-62:
(7*3)+(6*6)+(5*0)+(4*3)+(3*4)+(2*6)+(1*2)=95
95 % 10 = 5
So 36034-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2/c1-9-6-10(2)8-11(7-9)13-5-3-4-12/h6-8,13H,3,5H2,1-2H3
36034-62-5Relevant academic research and scientific papers
Indolyl or indolinyl derivatives and medicinal use thereof as ACAT or lipid peroxidation inhibitors
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, (2008/06/13)
PCT No. PCT/JP96/02852 Sec. 371 Date Apr. 3, 1998 Sec. 102(e) Date Apr. 3, 1998 PCT Filed Sep. 30, 1996 PCT Pub. No. WO97/12860 PCT Pub. Date Apr. 10, 1997A heterocyclic derivative of the formula (I) wherein each symbol is as defined in the specification,
Arylaminoalkylthioamides
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, (2008/06/13)
Arylaminoalkylthioamides and salts thereof wherein the benzene ring is substituted with halo, alkyl, lower alkoxy or 1,3-butadienylene are disclosed. The compounds are prepared by the reaction of the correspondingly substituted arylaminoalkylnitrile with
