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16062-68-3

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16062-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16062-68-3 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 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16062-68:
(7*1)+(6*6)+(5*0)+(4*6)+(3*2)+(2*6)+(1*8)=93
93 % 10 = 3
So 16062-68-3 is a valid CAS Registry Number.

16062-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-2-phenylbenzo[e][1,3]oxacin-4-one

1.2 Other means of identification

Product number -
Other names 2-Phenyl-6-nitro-3,1-benzoxazinon

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:16062-68-3 SDS

16062-68-3Relevant articles and documents

From Methaqualone and Beyond: Structure - Activity Relationship of 6-, 7-, and 8-Substituted 2,3-Diphenyl-quinazolin-4(3H)-ones and in Silico Prediction of Putative Binding Modes of Quinazolin-4(3H)-ones as Positive Allosteric Modulators of GABAA

Wang, Peng-Fei,Jensen, Anders A.,Bunch, Lennart

, p. 4362 - 4375 (2020/11/30)

Methaqualone (2-methyl-3-(o-tolyl)-quinazolin-4(3H)-one, MTQ) is a moderately potent positive allosteric modulator (PAM) of GABAA receptors (GABAARs). In a previous structure-activity relationship (SAR) study probing the importance of 2- and 3-substituent

Mechanochemical Synthesis of Substituted 4H-3,1-Benzoxazin-4-ones, 2-Aminobenzoxazin-4-ones, and 2-Amino-4H-3,1-benzothiazin-4-ones Mediated by 2,4,6-Trichloro-1,3,5-triazine and Triphenylphosphine

Pattarawarapan, Mookda,Wet-Osot, Sirawit,Yamano, Dolnapa,Phakhodee, Wong

, p. 589 - 592 (2017/03/11)

A mild and convenient approach for the synthesis of 2-substituted 4H-3,1-benzoxazin-4-ones, 2-aminobenzoxazin-4-ones, and 2-amino-4H-3,1-benzothiazin-4-ones under solvent-assisted grinding is reported. In the presence of 2,4,6-trichloro-1,3,5-triazine and

Synthesis, characterization, and pharmacological evaluation of 1-[2-(6-nitro-4-oxo-2-phenyl-4H-quinazolin-3-yl)-ethyl]-3-phenyl ureas

Rana, Aniruddhasinh M.,Desai, Kishor R.,Jauhari, Smita

, p. 225 - 233 (2013/03/13)

In the present communication, a series based on 1-[2-(6-nitro-4-oxo-2- phenyl-4H-quinazolin-3-yl)-ethyl]-3-phenyl-urea have been synthesized by an efficient synthetic protocol. The synthesized compounds were characterized by IR, 1H NMR, 13

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