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19181-64-7

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19181-64-7 Usage

General Description

6-Methoxyquinazolin-4-ol is a chemical compound with the molecular formula C9H7N3O2. It is a quinazolin-4-ol derivative, which means it has a quinazoline core structure with a hydroxyl group at the 4th position and an additional methoxy group at the 6th position. 6-METHOXYQUINAZOLIN-4-OL may have potential applications in the pharmaceutical industry, particularly in the development of drugs for various medical conditions. Its specific properties and potential uses would need to be further investigated through research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 19181-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,8 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19181-64:
(7*1)+(6*9)+(5*1)+(4*8)+(3*1)+(2*6)+(1*4)=117
117 % 10 = 7
So 19181-64-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H6O3/c1-3-5(7)4(6)2-8-3/h7H,2H2,1H3

19181-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-1H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 6-methoxy-4(3H)-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:19181-64-7 SDS

19181-64-7Relevant articles and documents

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Smith,Elisberg,Sherrill

, p. 1301 (1946)

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Electrosynthesis of CF3-Substituted Polycyclic Quinazolinones via Cascade Trifluoromethylation/Cyclization of Unactivated Alkene

He, Jiaying,Ling, Fei,Liu, Lei,Xu, Chao,Xu, Zhenhui,Yang, Zehui,Zhang, Wangqin,Zhong, Weihui

supporting information, (2022/03/15)

An atom and step economy cascade trifluoromethylation/cyclization of unactivated alkene with Langlois reagent as a CF3 source is described. A variety of polycyclic quinazolinones were successfully synthesized in 52–81% yields under transition metal- and oxidant-free conditions. The Langlois reagent used in this strategy as a CF3 reagent possesses the advantages of bench-stablity, cost-effectivity and high-efficiency. Additionally, gram-scale reaction, broad substrate scope and good functional group tolerance demonstrated the synthetic usefulness of this protocol.

Self-catalyzed phototandem perfluoroalkylation/cyclization of unactivated alkenes: Synthesis of perfluoroalkyl-substituted quinazolinones

Sun, Bin,Huang, Panyi,Yan, Zhiyang,Shi, Xiayue,Tang, Xiaoli,Yang, Jin,Jin, Can

supporting information, p. 1026 - 1031 (2021/02/06)

A novel visible-light-induced radical tandem trifluoromethylation/cyclization of unactivated alkenes with sodium perfluoroalkanesulfinates (Rf = CF3, C3F7, C4F9, C6F13, C8F17) under air atmosphere has been developed. A range of quinazolinones containing unactivated alkene moiety and sodium perfluoroalkanesulfinates were compatible with this transformation, leading to a variety of perfluoroalkyl-substituted quinazoline alkaloids. Remarkably, the experiment can be carried out without any metal catalyst, strong oxidant, or external photosensitizer.

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