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6-methoxy-4-phenyl-1-(2,2,2-trifluoroethyl)-2-(1H)-quinazolinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49830-89-9

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49830-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49830-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,3 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 49830-89:
(7*4)+(6*9)+(5*8)+(4*3)+(3*0)+(2*8)+(1*9)=159
159 % 10 = 9
So 49830-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H13F3N2O2/c1-24-12-7-8-14-13(9-12)15(11-5-3-2-4-6-11)21-16(23)22(14)10-17(18,19)20/h2-9H,10H2,1H3

49830-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-4-phenyl-1-(2,2,2-trifluoroethyl)quinazolin-2-one

1.2 Other means of identification

Product number -
Other names Moptfeq

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:49830-89-9 SDS

49830-89-9Downstream Products

49830-89-9Relevant academic research and scientific papers

Process for preparing 2(1H)-quinazolinone derivatives

-

, (2008/06/13)

2(1H)-Quinazolinone and quinazolinethione derivatives having excellent pharmacological activities are produced in high yield with high purity by heating the corresponding 3,4-dihydro-2(1H)-quinazolinone or quinazolinethione derivatives together with sulfur in an inert solvent.

1-Polyhaloalkyl-2(1H)-quinazolinone derivatives

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, (2008/06/13)

1-Polyhaloalkyl-2(1H)-quinazoline derivatives of the formula, STR1 wherein R is polyhaloalkyl having C2 -C4 alkyl; and R1, R2 and R3 are individually hydrogen, C1 -C4 alkyl, C1 -C4 alkoxy, nitro, trifluoromethyl or halogen, have excellent anti-inflammatory and analgesic activities with very low toxicity. These quinazolinone derivatives can be prepared, for example, by reacting a trihalogenoacetamidobenzophenone derivative with ammonia.

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