13961-64-3

• 

• Basic information

  1. Product Name: 6-Methyl-4-phenylquinazolin-2(1H)-one
  2. Synonyms: 6-Methyl-4-phenylquinazolin-2(1H)-one
  3. CAS NO:13961-64-3
  4. Molecular Formula: C₁₅H₁₂N₂O
  5. Molecular Weight: 236.26858
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13961-64-3.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: °Cat760mmHg
  3. Flash Point: °C
  4. Appearance: /
  5. Density: 1.21g/cm³
  6. Refractive Index: 1.648
  7. Storage Temp.: 2-8°C
  8. Solubility: N/A
  9. CAS DataBase Reference: 6-Methyl-4-phenylquinazolin-2(1H)-one(CAS DataBase Reference)
  10. NIST Chemistry Reference: 6-Methyl-4-phenylquinazolin-2(1H)-one(13961-64-3)
  11. EPA Substance Registry System: 6-Methyl-4-phenylquinazolin-2(1H)-one(13961-64-3)

• 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: 13961-64-3(Hazardous Substances Data)

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13961-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13961-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,6 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13961-64:
(7*1)+(6*3)+(5*9)+(4*6)+(3*1)+(2*6)+(1*4)=113
113 % 10 = 3
So 13961-64-3 is a valid CAS Registry Number.

InChI:InChI=1/C15H12N2O/c1-10-7-8-13-12(9-10)14(17-15(18)16-13)11-5-3-2-4-6-11/h2-9H,1H3,(H,16,17,18)

13961-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	6-methyl-4-phenyl-1H-quinazolin-2-one

1.2 Other means of identification

Product number	-
Other names	2(1H)-Quinazolinone,6-methyl-4-phenyl

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:13961-64-3 SDS

13961-64-3Upstream product

• 108-86-1 bromobenzene 
• 5925-93-9 2-amino-5-methylbenzonitrile 
• 541-41-3 chloroformic acid ethyl ester 
• 98-88-4 benzoyl chloride 
• 17852-28-7 2-amino-5-methylbenzophenone 
• 57-13-6 urea 

13961-64-3Downstream Products

13961-64-3Relevant articles and documents

Biomimetic Asymmetric Reduction of Quinazolinones with Chiral and Regenerable NAD(P)H Models

Zhao, Zi-Biao,Li, Xiang,Wu, Bo,Zhou, Yong-Gui

supporting information, p. 714 - 718 (2020/05/04)

A facile approach to chiral dihydroquinazolinone derivatives has been described via biomimetic asymmetric reduction of quinazolinones with chiral and regenerable NAD(P)H models. The utility of this method was demonstrated by a concise synthesis of the bromodomain protein divalent inhibitor.

Production of quinazolinone compounds

-

, (2008/06/13)

2(1H)-Quinazolinone derivatives, which are useful as anti-inflammatory agents, are prepared by heating or hydrolyzing an acylurea derivative. The acylurea derivative can be prepared by either reacting an indole derivative with an oxidizing agent or reacti

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