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Butanoic acid, 2-[[4-(6-bromo-2-methyl-4-oxo-3(4H)-quinazolinyl)phenyl]hydrazono]-3- oxo-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

662142-45-2

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662142-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 662142-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,2,1,4 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 662142-45:
(8*6)+(7*6)+(6*2)+(5*1)+(4*4)+(3*2)+(2*4)+(1*5)=142
142 % 10 = 2
So 662142-45-2 is a valid CAS Registry Number.

662142-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-{[4-(6-bromo-2-methyl-4-oxo-4H-quinazolin-3-yl)phenyl]hydrazono}-3-oxobutyric acid ethyl ester

1.2 Other means of identification

Product number -
Other names 2-{[4-(6-Bromo-2-methyl-4-oxo-4H-quinazolin-3-yl)-phenyl]-hydrazono}-3-oxo-butyric acid ethyl ester

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:662142-45-2 SDS

662142-45-2Downstream Products

662142-45-2Relevant academic research and scientific papers

Synthesis of novel 3H-quinazolin-4-ones containing pyrazolinone, pyrazole and pyrimidinone moieties

Saleh, Mohamed A.,Abdel-Megeed, Mohamed F.,Abdo, Mohamed A.,Shokr, Abdel-Basset M.

, p. 363 - 373 (2007/10/03)

The diazonium salt of 3-(4-aminophenyl)-2-methyl-3H-quinazolin-4-one (2a) and its 6-bromo derivative 2b reacted with some active methylene compounds, namely ethyl acetoacetate (3), ethyl cyanoacetate (4) and acetylacetone (5), to afford the corresponding hydrazono quinazolinone derivatives 6-8. Treatment of 6a,b with hydrazine hydrate or phenyl hydrazine in refluxing ethanol afforded the corresponding pyrazolin-5-one derivatives of 3H-quinazolin-4-one 9a-d. Cyclization of 7a,b with hydrazine hydrate yielded the corresponding products 10a,b. Reaction of 8a,b with phenyl hydrazine or with urea afforded the corresponding derivatives 11a,b and 12a,b, respectively. Compounds 6-12 were identified by C,H,N analysis, IR, 1H-NMR, 13C-NMR and mass spectroscopy.

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