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6-methyl-2-(p-tolylamino)quinazolin-4(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79714-12-8 Structure
  • Basic information

    1. Product Name: 6-methyl-2-(p-tolylamino)quinazolin-4(3H)-one
    2. Synonyms: 6-methyl-2-(p-tolylamino)quinazolin-4(3H)-one
    3. CAS NO:79714-12-8
    4. Molecular Formula:
    5. Molecular Weight: 265.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79714-12-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-methyl-2-(p-tolylamino)quinazolin-4(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-methyl-2-(p-tolylamino)quinazolin-4(3H)-one(79714-12-8)
    11. EPA Substance Registry System: 6-methyl-2-(p-tolylamino)quinazolin-4(3H)-one(79714-12-8)
  • 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: 79714-12-8(Hazardous Substances Data)

79714-12-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79714-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,1 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79714-12:
(7*7)+(6*9)+(5*7)+(4*1)+(3*4)+(2*1)+(1*2)=158
158 % 10 = 8
So 79714-12-8 is a valid CAS Registry Number.

79714-12-8Downstream Products

79714-12-8Relevant articles and documents

Regioselective synthesis and biological evaluation of: N -substituted 2-aminoquinazolin-4-ones

Liao, Zhen-Yuan,Yeh, Wen-Hsiung,Liao, Pen-Yuan,Liu, Yu-Ting,Chen, Ying-Cheng,Chen, Yi-Hung,Hsieh, Tsung-Han,Lin, Chia-Chi,Lu, Ming-Hsuan,Chen, Yi-Song,Hsu, Ming-Chih,Li, Tsai-Kun,Chien, Tun-Cheng

supporting information, p. 4482 - 4494 (2018/06/29)

The reaction of methyl anthranilates with N-arylcyanamides in the presence of p-TsOH in t-BuOH under reflux afforded predominantly 3-arylquinazolin-4-ones. In contrast, the reaction of the same reactants with TMSCl in t-BuOH at 60 °C followed by the Dimro

Investigation into a By-product from the Reaction of 2-Amino-5-methylbenzoic Acid with Ammonium Thiocyanate

Kennewell, Peter D.,Scrowston, Richard M.,Shenouda, Ibrahim G.,Tully, W. Roger,Westwood, Robert

, p. 2001 - 2025 (2007/10/02)

One of the by-products from the reaction of 2-amino-5-methylbenzoic acid with ammonium thiocyanate is shown to be 2,3-dihydro-5-methyl-2-thioxo-3-p-tolylquinazolin-4(1H)-one (6).This reacts with hydrazine to give three products (21)-(23), which have been converted into tetrazolo- (27) and 1,2,4-triazolo-quinazolino-derivatives (20) and (30).The products from the reaction of o-aminoacetophenone with an aryl isothiocyanate are converted into a reactive 1-azabuta-1,3-diene intermediate (34), which undergoes a ? cycloaddition reaction with dimethyl acetylenedicarboxylate, followed by a retro-Diels-Alder reaction, to give dimethyl 4-methylquinoline-2,3-dicarboxylate.

A NOVEL SYNTHESIS OF 2-SUBSTITUTED QUINAZOLIN-4(3H)-ONES

Svetlik, Jan

, p. 1281 - 1285 (2007/10/02)

Aromatic or mixed carbodiimides and ketenimines react with ethyl allophanate to give corresponding substituted quinazolin-4(3H)-ones.

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