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7-Chloro-2-chloroMethyl-1H-quinazolin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

730951-40-3

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730951-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 730951-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,0,9,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 730951-40:
(8*7)+(7*3)+(6*0)+(5*9)+(4*5)+(3*1)+(2*4)+(1*0)=153
153 % 10 = 3
So 730951-40-3 is a valid CAS Registry Number.

730951-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-2-(chloromethyl)-1H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 2-chloromethyl-7-chloroquinazolin-4(3H)-one

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:730951-40-3 SDS

730951-40-3Relevant academic research and scientific papers

Quinazolin-4(3H)-one based agents bearing thiadiazole-urea: Synthesis and evaluation of anti-proliferative and antiangiogenic activity

Faraji, Aram,Motahari, Rasoul,Hasanvand, Zaman,Oghabi Bakhshaiesh, Tayebeh,Toolabi, Mahsa,Moghimi, Setareh,Firoozpour, Loghman,Boshagh, Mohammad Amin,Rahmani, Roya,Ketabforoosh, Shima H.M.E.,Bijanzadeh, Hamid Reza,Esmaeili, Rezvan,Foroumadi, Alireza

, (2021/01/04)

A series of quinazolin-4(3H)-one based agents containing thiadiazole-urea were designed, synthesized, and biologically evaluated. The proliferation rate of PC3 cells was moderately reduced by compound 9f (IC50 = 17.7 μM)which was comparable with sorafenib (IC50 = 17.3 μM). There was also a significant reduction in the number of HUVEC cells, when they were exposed to compound 9y (IC50 = 6.1 μM). To test the potential of compounds in inducing apoptosis, Annexin V-FITC/propidium iodide double staining assay was used. After the treatment of HUVEC cells with 9f, they underwent apoptotic effects. A substantial effort was dedicated to gathering comprehensive data across CAM assay. These data showed that 9f moderately inhibits the growth of corresponding blood vessels. Finally, the outcomes of Western blotting proposed a mechanism of action, by which the phosphorylation of VEGFR-2 is inhibited by compounds 9f and 9y.

QUINAZOLINE BASED RESPIRATORY SYNCYTIAL VIRUS INHIBITORS

-

Page/Page column 53, (2015/05/19)

Compounds of Formula (I), wherein R1, R2, R3, R4 and n are defined herein, are useful as inhibitors of RSV.

BENZOXAZINONE DERIVATIVES FOR THE TREATMENT OF GLYTL MEDIATED DISORDERS

-

Page/Page column 91, (2011/02/24)

The present invention relates to benzoxazinone derivatives, processes for their preparation, pharmaceutical compositions and medicaments containing them and to their use in treating disorders mediated by GlyT1, including neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder.

A General synthetic procedure for 2-chloromethyl-4(3H)-quinazolinone derivatives and their utilization in the preparation of novel anticancer agents with 4-anilinoquinazoline scaffolds

Li, Hong-Ze,He, Hai-Yun,Han, Yuan-Yuan,Gu, Xin,He, Lin,Qi, Qing-Rong,Zhao, Ying-Lan,Yang, Li

experimental part, p. 9473 - 9485 (2011/02/27)

In our ongoing research on novel anticancer agents with 4-anilinoquinazoline scaffolds, a series of novel 2-chloromethyl-4(3H)- quinazolinones were needed as key intermediates. An improved one-step synthesis of 2-chloromethyl-4(3H)-quinazolinones utilizin

Regioselective Suzuki-Miyaura reaction: Application to the microwave-promoted synthesis of 4,7-diarylquinazolines

Kabri, Youssef,Verhaeghe, Pierre,Gellis, Armand,Vanelle, Patrice

scheme or table, p. 2949 - 2961 (2010/09/03)

New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions.

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