74878-32-3 Usage
Synonyms
4-amino-3,5-dichlorobenzyl alcohol
N-(3,5-dichloro-4-hydroxyphenyl)-4-aminoaniline
Physical Description
White to off-white crystalline powder
Functional Groups
Phenol group (benzenemethanol)
Aniline group (4-aminoaniline)
Chlorine atoms attached to the benzene ring
Applications
Synthesis of pharmaceuticals
Production of dyes
Organic compound synthesis
Potential applications in antiseptics and disinfectants
Health Hazards
Careful handling required due to potential health hazards
Reactivity
Reactivity should be taken into consideration during handling
Potential Uses
Production of antiseptics
Manufacturing pharmaceutical products
Check Digit Verification of cas no
The CAS Registry Mumber 74878-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,7 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74878-32:
(7*7)+(6*4)+(5*8)+(4*7)+(3*8)+(2*3)+(1*2)=173
173 % 10 = 3
So 74878-32-3 is a valid CAS Registry Number.
74878-32-3Relevant articles and documents
HETEROAROMATIC COMPOUNDS AS INHIBITORS OF STEAROYL-COENZYME A DELTA-9 DESATURASE
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Page/Page column 21, (2011/07/06)
Heteroaromatic compounds of structural formula I are selective inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD1) relative to other known stearoyl-coenzyme A desaturases. The compounds of the present invention are useful for the prevention and tr
HETEROAROMATIC COMPOUNDS AS INHIBITORS OF STEAROYL-COENZYME A DELTA-9 DESATURASE
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Page/Page column 40-41, (2010/04/27)
Heteroaromatic compounds of structural formula (I) are inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD). The compounds of the present invention are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and met
An Efficient Synthesis of Chloroethylclonidine
Zhang, Wei-Yi,Bakthavachalam, Venkatesalu,Gao, Yigong,White, William L.,Neumeyer, John L.
, p. 19 - 22 (2007/10/02)
An efficient pathway for the preparation of chloroethylclonidine dihydrochloride (1) is described.