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501105-12-0

N-{[2-(4-methylbenzoyl)hydrazino]carbonothioyl}benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 501105-12-0 Structure

  • Basic information

    1. Product Name: N-{[2-(4-methylbenzoyl)hydrazino]carbonothioyl}benzamide
    2. Synonyms: N-{[2-(4-methylbenzoyl)hydrazino]carbonothioyl}benzamide;N-({2-[(4-methylphenyl)carbonyl]hydrazinyl}carbonothioyl)benzamide
    3. CAS NO:501105-12-0
    4. Molecular Formula: C16H15N3O2S
    5. Molecular Weight: 313.3742
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 501105-12-0.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: N-{[2-(4-methylbenzoyl)hydrazino]carbonothioyl}benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-{[2-(4-methylbenzoyl)hydrazino]carbonothioyl}benzamide(501105-12-0)
    11. EPA Substance Registry System: N-{[2-(4-methylbenzoyl)hydrazino]carbonothioyl}benzamide(501105-12-0)

  • 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: 501105-12-0(Hazardous Substances Data)

501105-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501105-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,1,0 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501105-12:
(8*5)+(7*0)+(6*1)+(5*1)+(4*0)+(3*5)+(2*1)+(1*2)=70
70 % 10 = 0
So 501105-12-0 is a valid CAS Registry Number.

501105-12-0Downstream Products

501105-12-0Relevant articles and documents

A useful synthesis of 2-acylamino-1,3,4-oxadiazoles from acylthiosemicarbazides using potassium iodate and the discovery of new antibacterial compounds

Li, Tianlei,Wen, Gang,Li, Jishun,Zhang, Wenxuan,Wu, Song

, (2019/05/02)

A useful method for the synthesis of 2-acylamino-1,3,4-oxadiazoles was developed. By using potassium iodate as an oxidant in water at 60 ?C, a wide range of 2-acylamino-1,3,4-oxadiazoles were afforded in moderate to excellent yields within two

Intramolecular hydrogen bonding and anion binding of N-benzamido-N′- benzoylthioureas

Liu, Wen-Xia,Jiang, Yun-Bao

, p. 1124 - 1127 (2008/09/18)

(Chemical Equation Presented) N-(p-Dimethylamino)benzoyl-N′- phenylthiourea as an N-acylthiourea is known to be unable to bind anions due to a strong intramolecular hydrogen bond (IHB). We show here that by inserting an amido group in the N′-phenyl side the newly designed N-benzamido-N′- benzoylthioureas, despite this IHB too, bind strongly to anions with binding constants on the order of 106-107 mol-1 L. Results suggest that potential anion receptors or organocatalysts could be developed on the basis of this framework with a wide structural diversity.

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