16064-24-7

• 

• Basic information

  1. Product Name: 7-METHOXY-4(1H)-QUINAZOLINONE
  2. Synonyms: 7-METHOXY-4(1H)-QUINAZOLINONE;4(3H)-Quinazolinone, 7-methoxy-;7-Methoxyquinazolin-4(1H)-one;7-Methoxyquinazolin-4(3H)-one
  3. CAS NO:16064-24-7
  4. Molecular Formula: C₉H₈N₂O₂
  5. Molecular Weight: 176.17202
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 16064-24-7.mol
  9. Article Data: 23

• Chemical Properties

  1. Melting Point: 257-258℃
  2. Boiling Point: 338.7 °C at 760 mmHg
  3. Flash Point: 158.7 °C
  4. Appearance: /
  5. Density: 1.32
  6. Refractive Index: N/A
  7. Storage Temp.: 2-8°C
  8. Solubility: N/A
  9. PKA: 1.51±0.20(Predicted)
  10. CAS DataBase Reference: 7-METHOXY-4(1H)-QUINAZOLINONE(CAS DataBase Reference)
  11. NIST Chemistry Reference: 7-METHOXY-4(1H)-QUINAZOLINONE(16064-24-7)
  12. EPA Substance Registry System: 7-METHOXY-4(1H)-QUINAZOLINONE(16064-24-7)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 16064-24-7(Hazardous Substances Data)

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• 7-METHOXYQUINAZOLIN-4(1H)-ONE

  Cas No: 16064-24-7

• USD $ 3.0-3.0 / Kilogram

• 1 Kilogram

• 1-100 Metric Ton/Month

• Dayang Chem (Hangzhou) Co.,Ltd.
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• 4(3H)-Quinazolinone,7-methoxy-

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• Hangzhou J&H Chemical Co., Ltd.
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• 4(3H)-Quinazolinone,7-methoxy-

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• 10 Gram

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• 7-METHOXY-4(1H)-QUINAZOLINONE Cas no.16064-24-7 98%

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16064-24-7 Usage

General Description

7-METHOXY-4(1H)-QUINAZOLINONE is a chemical compound with the molecular formula C9H8N2O2. It is a derivative of quinazolinone, a nitrogen-containing heterocyclic compound. 7-METHOXY-4(1H)-QUINAZOLINONE is commonly used in medicinal chemistry for its potential pharmacological properties, such as anti-cancer, anti-inflammatory, and analgesic activities. It has shown to have some promising effects in preclinical studies and is being researched for its therapeutic potential. Its structure and properties make it a promising target for drug development and further research into its potential applications in the field of medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 16064-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,6 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16064-24:
(7*1)+(6*6)+(5*0)+(4*6)+(3*4)+(2*2)+(1*4)=87
87 % 10 = 7
So 16064-24-7 is a valid CAS Registry Number.

16064-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	7-Methoxyquinazolin-4(1H)-one

1.2 Other means of identification

Product number	-
Other names	7-methoxy-1H-quinazolin-4-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:16064-24-7 SDS

16064-24-7Upstream product

• 50413-30-4 methyl 2-amino-4-methoxybenzoate 
• 77287-34-4 formamide 
• 4294-95-5 4-methoxyanthranilic acid 
• 463-52-5 formamidine 
• 3473-63-0 formamidine acetic acid 
• 38469-83-9 4-methoxy-2-nitro-benzonitrile 
• 33844-22-3 4-methoxy-2-nitro-benzoic acid amide 
• 64-18-6 formic acid 
• 38487-91-1 2-amino-p-anisamide 

16064-24-7Downstream Products

• 55496-52-1 4-chloro-7-methoxy-quinazoline 
• 16064-25-8 7-hydroxyquinazoline-4(3H)-one 
• 1613479-53-0 C₁₅H₁₀F₂N₂O₂ 

16064-24-7Relevant articles and documents

Photo-Triggered Self-Induced Homolytic Dechlorinative Sulfonylation/Cyclization of Unactivated Alkenes: Synthesis of Quinazolinones Containing a Sulfonyl Group

Sun, Bin,Ding, Hao,Tian, Hai-Xia,Huang, Pan-Yi,Jin, Can,Wu, Chun-Lei,Shen, Run-Pu

supporting information, p. 766 - 772 (2021/12/22)

A self-photocatalyzed sulfonylation/cyclization of quinazolinones containing unactivated alkenes with various sulfonyl chlorides was developed. The protocol provides access to sulfonyl radicals via energy transfer from the quinazolinone skeleton to the sulfonyl chloride. Notably, the transformations proceeded without any external photocatalysts, additives, or oxidants, providing an alternative method for fabricating sulfonylated compounds.

Visible-Light Photosynthesis of CHF2/CClF2/CBrF2-Substituted Ring-fused Quinazolinones in Dimethyl Carbonate

Gui, Qing-Wen,He, Wei-Min,Huang, Wen-Jie,Lu, Zi-Qin,Ouyang, Wen-Tao,Teng, Fan,Xun, Changping,Yang, Hao,Zhu, Meng-Xue

, (2021/12/01)

With eco-friendly and sustainable CO2-derived dimethyl carbonate as the sole solvent, the visible-light-induced cascade radical reactions have been established as a green and efficient tool for constructing various CHF2/CClF2/CBrF2-substituted ring-fused quinazolinones.

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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