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4(1H)-Quinazolinone, 2,3-dihydro-1-methyl-3-(phenylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95757-92-9

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95757-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95757-92-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,5 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95757-92:
(7*9)+(6*5)+(5*7)+(4*5)+(3*7)+(2*9)+(1*2)=189
189 % 10 = 9
So 95757-92-9 is a valid CAS Registry Number.

95757-92-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-anilino-1-methyl-2H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 4(1H)-Quinazolinone,2,3-dihydro-1-methyl-3-(phenylamino)

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:95757-92-9 SDS

95757-92-9Relevant academic research and scientific papers

Synthesis of new benzotriazepin-5(2H)-one derivatives of expected antipsychotic activity

Ibrahim, Samy M.,Baraka, Mohamed M.,El-Sabbagh, Osama I.,Kothayer, Hend

, p. 1488 - 1496 (2013/04/10)

A new series of 3,4-dihydro-1H-benzo[e][1,2,4]triazepin-5(2H)-one derivatives were synthesized by cyclocondensation of benzohydrazides (II, IX), derived from the reaction of N-methyl-isatoic anhydride with phenyl hydrazine and isonicotinic acid hydrazide, respectively, with formaldehyde, aromatic aldehydes in acidic medium or with carbon disulfide in alkaline medium, the last reaction was only carried out with benzohydrazide II. Benzotriazepinone derivatives IV,V a-h,VI, and XI were subjected to ptosis test using clozapine as a reference drug to evaluate their antipsychotic activity. It was found that 2-thioxobenzotriazepinone VI had the same antipsychotic activity as reference drug clozapine but with lesser side effects whereas it showed nonsignificant CNS depressant activity upon using forced swim pool test as well as no neurotoxicity when tested in mice using rotarod or horizontal screen tests. Graphical Abstract: A new series of benzotriazepin-5(2H)-ones (IV,V a-h, VI, and XI) were prepared starting from isatoic anhydride and their antipsychotic activity revealed that 2-thioxobenzotriazepinone VI was superior to the reference drug clozapine.[Figure not available: see fulltext.]

Composes Sulfures Heterocycliques. CIII. Action de la phenylhydrazine sur les dihydro-1,2 benzothiazine-3,1 thiones-4

Legrand, Louis,Lozac'h, Nooel

, p. 1625 - 1632 (2007/10/02)

While phenylhydrazine reacts with 1-alkyl-1,2-dihydro-3,1-benzothiazine-4-thiones (1) giving 1-alkyl-3-phenylamino-2,3-dihydro-1H-quinazoline-4-thiones (2), it reacts with 1-aryl-1,2-dihydro-3,1-benzothiazine-4-thiones (3) yielding 1-aryl-4-phenylhydrazon

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