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3-[2-(2,5-dihydroxyphenyl)ethyl]-2-phenylquinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86804-50-4

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86804-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86804-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,0 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86804-50:
(7*8)+(6*6)+(5*8)+(4*0)+(3*4)+(2*5)+(1*0)=154
154 % 10 = 4
So 86804-50-4 is a valid CAS Registry Number.

86804-50-4SDS

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 3-(2,5-dihydroxyphenethyl)-2-phenylquinazolin-4(3H)-one

1.2 Other means of identification

Product number -
Other names -

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:86804-50-4 SDS

86804-50-4Relevant academic research and scientific papers

Synthesis and antiviral activity of some novel substituted phenothiazines

Pandey,Saxena,Joshi,Bajpai

, p. 1015 - 1017 (2007/10/03)

Hydroquinone on reaction with amido alcohols 1 in the presence of conc. H2SO4 gives 2-arylamido/imidoalkyl-1,4-dihydroxy-benzenes 2 which undergo cyclization with aromatic primary amine and sulphur in the presence of iodine to yield 2-arylamido/imidoalkyl-10H-phenothiazin-3-ols 3. Compounds 3 are further substituted to 2-arylamido/imidoalkyl-10-[(4- methoxyphenyl/phenyl) phenylamino-methyl]-10H-phenothiazin-3-ols 4. Compounds 4 have been screened for their antiviral activity against Japanese encephalitis virus (JEV) and Herpes simplex virus type-I (HSV-I).

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