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329080-15-1

3-amino-2-(2-thienyl)-4(3H)-quinazolinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 329080-15-1 Structure

  • Basic information

    1. Product Name: 3-amino-2-(2-thienyl)-4(3H)-quinazolinone
    2. Synonyms: 3-amino-2-(2-thienyl)-4(3H)-quinazolinone
    3. CAS NO:329080-15-1
    4. Molecular Formula: C12H9N3OS
    5. Molecular Weight: 243.28436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 329080-15-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-amino-2-(2-thienyl)-4(3H)-quinazolinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-amino-2-(2-thienyl)-4(3H)-quinazolinone(329080-15-1)
    11. EPA Substance Registry System: 3-amino-2-(2-thienyl)-4(3H)-quinazolinone(329080-15-1)

  • 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: 329080-15-1(Hazardous Substances Data)

329080-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329080-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,0,8 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 329080-15:
(8*3)+(7*2)+(6*9)+(5*0)+(4*8)+(3*0)+(2*1)+(1*5)=131
131 % 10 = 1
So 329080-15-1 is a valid CAS Registry Number.

329080-15-1Downstream Products

329080-15-1Relevant articles and documents

Development of certain novel N-(2-(2-(2-oxoindolin-3-ylidene)hydrazinecarbonyl)phenyl)-benzamides and 3-(2-oxoindolin-3-ylideneamino)-2-substituted quinazolin-4(3 H)-ones as CFM-1 analogs: Design, synthesis, QSAR analysis and anticancer activity

Alafeefy, Ahmed M.,Ashour, Abdelkader E.,Prasad, Onkar,Sinha, Leena,Pathak, Shilendra,Alasmari, Fatimah A.,Rishi, Arun K.,Abdel-Aziz, Hatem A.

, p. 191 - 201 (2015/06/02)

The reaction of N-(2-(hydrazinecarbonyl)aryl)benzamides 2a, b with indoline-2,3-diones 4ae in acidified ethanolic solution furnished the corresponding N-(2-(2-(2-oxoindolin-3-ylidene)hydrazinecarbonyl)phenyl)benzamides 5aj, respectively. Furthermore, 3-(2

Synthesis of derivatives of thiophene using methyl 2-isothiocyanatobenzoate

Deck,Turner,Deck,Papadopoulos

, p. 343 - 347 (2007/10/03)

A variety of 2-substituted thiophenes is readily obtained from 2-(2-thienyl)-4H-3,1-benzothiazin-4-one (2), which is formed when thiophene reacts with methyl 2-isothiocyanatobenzoate (1) in the presence of anhydrous stannic chloride.

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