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53929-76-3

Benzamide, 2-hydroxy-4-methoxy-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53929-76-3 Structure

  • Basic information

    1. Product Name: Benzamide, 2-hydroxy-4-methoxy-N-phenyl-
    2. Synonyms:
    3. CAS NO:53929-76-3
    4. Molecular Formula: C14H13NO3
    5. Molecular Weight: 243.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53929-76-3.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: Benzamide, 2-hydroxy-4-methoxy-N-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, 2-hydroxy-4-methoxy-N-phenyl-(53929-76-3)
    11. EPA Substance Registry System: Benzamide, 2-hydroxy-4-methoxy-N-phenyl-(53929-76-3)

  • 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: 53929-76-3(Hazardous Substances Data)

53929-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53929-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,2 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53929-76:
(7*5)+(6*3)+(5*9)+(4*2)+(3*9)+(2*7)+(1*6)=153
153 % 10 = 3
So 53929-76-3 is a valid CAS Registry Number.

53929-76-3Relevant articles and documents

Relationship between the structure and antimycobacterial activity of substituted salicylanilides

Waisser, Karel,Bures, Otakar,Holy, Pavel,Kunes, Jiri,Oswald, Radek,Jiraskova, Lucie,Pour, Milan,Klimesova, Vera,Kubicova, Lenka,Kaustova, Jarmila

, p. 53 - 71 (2007/10/03)

A series of 143 salicylanilides substituted in positions 4 and 5 and in positions 3′ and 4′ was synthesized. The compounds were evaluated for in vitro antimycobacterial activity against Mycobacterium tuberculosis, Mycobacterium kansasii, and Mycobacterium

Synthesis of Substituted Salicylanilides under Microwave Irradiation

Veverkova, Eva,Meciarova, Maria,Toma, Stefan,Balko, Jozef

, p. 1215 - 1219 (2007/10/03)

Salicylanilides were prepared in 70-95% yields in 4-8 min from phenyl salicylate or phenyl 4-methoxysalicylate and substituted anilines under microwave irradiation under solvent free conditions.

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