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6-AMINO-2-METHYL-QUINAZOLIN-4-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17329-24-7

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17329-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17329-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,2 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17329-24:
(7*1)+(6*7)+(5*3)+(4*2)+(3*9)+(2*2)+(1*4)=107
107 % 10 = 7
So 17329-24-7 is a valid CAS Registry Number.

17329-24-7SDS

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-amino-2-methyl-1H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 6-amino-3,4-dihydro-2-methyl-4-oxoquinazoline

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:17329-24-7 SDS

17329-24-7Downstream Products

17329-24-7Relevant academic research and scientific papers

Synthesis and antiproliferative evaluation of hybrids of indolin-2-one and quinazoline-4(3H)-one linked via imine bond

Wu, Wei-Yao,Cao, Sheng-Li,Mao, Bei-Bei,Liao, Ji,Li, Zhong-Feng,Song, Hao-Bin,Xu, Xingzhi

, p. 61 - 66 (2013/08/22)

A novel series of hybrids of indolin-2-one and quinazolin-4(3H)-one linked via an imine bond were synthesized and tested for their inhibitory activity against the proliferation of a panel of five human cancer cell lines. We found that compound 5c bearing

BICYCLIC LACTAM FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS

-

Page/Page column 133-134, (2008/12/07)

The present invention provides novel bicyclic lactams derivatives, and analogues thereof, of Formula (I): or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate, or prodrug thereof, wherein the variables A, B, C, W, Y, Z1, Z2, Z3, Z4, R8, and R9 are as defined herein. These compounds are selective inhibitors of factor VIIa which can be used as medicaments.

Quinazoline Antifolate Thymidylate Synthase Inhibitors: Bridge Modifications and Conformationally Restricted Analogues in the C-2-Methyl Series

Marsham, Peter R.,Jackman, Ann L.,Hayter, Anthony J.,Daw, Melanie R.,Snowden, Jayne L.,et al.

, p. 2209 - 2218 (2007/10/02)

Several C2-methylquinazoline-based antifolates (14-26) have been prepared in which the C9,N10 bridge has been replaced by the reversed N9,C10 unit.This series was extensively studied by incorporating further substituents at N9 and C10 as well as by modifications to the p-aminobenzoate ring.The C-2-methylquinazoline analogues 29, 30, and 31 containing the methyleneoxa, methylenethia, and thia bridge units were also synthesized.In general these isosteric replacements of the bridge unit in the parent C2-methyl-N10-propargylquinazoline antifolate 2 were much less potent as inhibitors of isolated thymidylate synthase (TS) but several were at least as potent as inhibitors of L1210 cell growth in culture.The fusion of the p-aminobenzoate ring into the bicyclic systems 75 and 76 also reduced activity against TS but again gave highly cytotoxic compounds.The cytotoxicities were largely prevented by thymidine, confirming that TS in the major locus.

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