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4(3H)-Quinazolinone, 3-(4-acetylphenyl)-6,8-dibromo-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70298-45-2

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70298-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70298-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,9 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 70298-45:
(7*7)+(6*0)+(5*2)+(4*9)+(3*8)+(2*4)+(1*5)=132
132 % 10 = 2
So 70298-45-2 is a valid CAS Registry Number.

70298-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-acetylphenyl)-6,8-dibromo-2-methylquinazolin-4-one

1.2 Other means of identification

Product number -
Other names 2-Methyl-6,8-dibromo-3-(4'-acetylphenyl)-4-quinazolinone

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:70298-45-2 SDS

70298-45-2Relevant academic research and scientific papers

Synthesis and studies of the behaviour of 6,8-Dibromo-2-substituted 4H-3,1-benzoxazin-4-ones

Kassab, R. R.,El-Hashash, M. A.,Ahmad, I. GH.

, p. 487 - 500 (2007/10/03)

The title compounds 1a-c were prepared via reaction of 3,5-dibromo anthranilic acid with acetic anhydride, succinic anhydride and/or maleic anhydride. Reaction of 1a-c with hydrazine hydrate yielded the corresponding 3-amino quinazoline derivatives 2a-c. The reaction of 2a and/or 2b with aromatic aldehydes, namely 2,4-dichlorobenzaldehyde, 4-hydroxybenzaldehyde, and/or 4-methoxybenzaldehyde gave 3a-c, while the reaction of 1b with 2,4-dichlorobenzaldehyde in the presence of anhydrous ZnCl2 yielded 4. But when compound 2b was reacted with 2,4-dichlorobenzaldehyde in the presence of AcOH/Ac2O yielded 5, which was formed also when compound 4 was reacted with N2H4 in boiling ethanol. Treatment of compound 2c with maleic anhydride gave 6. On the other hand, 1a was reacted with 4-aminoacetophenone to give compound 7, and with NaN3 to give 9 and 10. The reaction of 1a with sulphadrugs afforded 11a-d. The structures of the new compounds were confirmed by analytical and different spectroscopic methods. The various compounds prepared are outlined in schemes 1 and 2. Significant antimicrobial activities were observed for some members of the series.

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