6953-32-8 Usage
Description
(4E)-N-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-4H-chromen-4-imine is a complex chemical compound characterized by its imine functional group and a chromen-4-imine moiety. It also includes a methoxyphenyl substituent and a hydroxyl group, which may contribute to its potential interactions with biological molecules. (4E)-N-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-4H-chromen-4-imine could possess pharmacological or physiological activity, warranting further investigation into its properties and possible applications.
Uses
Used in Pharmaceutical Industry:
(4E)-N-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-4H-chromen-4-imine is used as a potential pharmaceutical agent for its possible pharmacological activity. The presence of the imine group and the hydroxyl group may allow it to interact with biological targets, suggesting its use in the development of new drugs or therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (4E)-N-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-4H-chromen-4-imine serves as a subject of study for understanding the properties and reactivity of complex molecular structures. Its unique features may provide insights into new chemical reactions or mechanisms, contributing to the advancement of synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6953-32-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6953-32:
(6*6)+(5*9)+(4*5)+(3*3)+(2*3)+(1*2)=118
118 % 10 = 8
So 6953-32-8 is a valid CAS Registry Number.
6953-32-8Relevant articles and documents
Synthesis and cytotoxicity of novel (E)-2-phenylchroman-4-one-O-((1-substituted-1H-1,2,3-triazol-4-yl)methyl) oxime derivatives
Gutam, Madhu,Mokenapelli, Sudhakar,Yerrabelli, Jayaprakash Rao,Banerjee, Somesh,Roy, Partha,Chitneni, Prasad Rao
, p. 1883 - 1891 (2020/05/13)
A series of new flavanone-triazole hybrids (7a–m) were synthesized from flavanone oximes (6a–c) via multistep synthetic strategy, involving Cu (I) catalyzed azide, alkyne 1,3-dipolar cycloaddition by Click reaction. All the synthesized compounds were tested for their cytotoxicity against HCT-15, HeLa, NCI-H522, and HEK-293 (normal cell line) cell lines. Compounds 6a, 7a, 7b, 7d, 7e, 7j, and 7m showed the significant cytotoxicity, wherein compound 7b showed potential cytotoxicity against NCI-H522 cell line and compounds 6a and 7a were offensive with HEK-293 in their toxicity profile.
CHALCONE OXIMES. PART V. REACTION OF HYDROXYLAMINE WITH 4-SUBSTITUTED 2'-HYDROXYCHALCONES
Witczak, Zbigniew,Krolikowska, Maria
, p. 89 - 100 (2007/10/02)
The reactions of hydroxylamine with 4-substituted 2'-hydroxychalcones have been investigated.Formation of products of 1,2 addition and simultaneous 1,4 and 1,2 addition for R = -CH3, -Cl have been established.Products of 1,2 addition for R = -OCH3 and of
