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5-(2-amino-thiazol-5-yl)-2-hydroxy-benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 799280-23-2 Structure
  • Basic information

    1. Product Name: 5-(2-amino-thiazol-5-yl)-2-hydroxy-benzamide
    2. Synonyms: 5-(2-amino-thiazol-5-yl)-2-hydroxy-benzamide
    3. CAS NO:799280-23-2
    4. Molecular Formula:
    5. Molecular Weight: 235.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 799280-23-2.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: 5-(2-amino-thiazol-5-yl)-2-hydroxy-benzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(2-amino-thiazol-5-yl)-2-hydroxy-benzamide(799280-23-2)
    11. EPA Substance Registry System: 5-(2-amino-thiazol-5-yl)-2-hydroxy-benzamide(799280-23-2)
  • 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: 799280-23-2(Hazardous Substances Data)

799280-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 799280-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,9,2,8 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 799280-23:
(8*7)+(7*9)+(6*9)+(5*2)+(4*8)+(3*0)+(2*2)+(1*3)=222
222 % 10 = 2
So 799280-23-2 is a valid CAS Registry Number.

799280-23-2Downstream Products

799280-23-2Relevant articles and documents

Synthesis of some new 5-(2-substituted-1,3-thiazol-5-yl)-2-hydroxy benzamides and their 2-alkoxy derivatives as possible antifungal agents

Narayana,Vijaya Raj,Ashalatha,Kumari, N. Suchetha,Sarojini

, p. 867 - 872 (2007/10/03)

The 2-hydroxy-5-(1,3-thiazol-5-yl) benzamide (4a), 5-(2-amino-1, 3-thiazol-5-yl)-2-hydroxy benzamide (4b), 2-hydroxy-5-(2-alkyl-1,3-Thiazol-5-yl) benzamide (4c and 4d), 5-{2-[(N-substituted aryl)amino]-1,3-thiazol-5-yl}2- hydroxy benzamides (6a-j) were prepared by reacting 5-(bromoacetyl) salicylamide (2) with thiourea, thioformamide, thioalkylamide (3c-d) and substituted thioureas (5a-j) in absolute ethanol. These compounds were converted to 5-(2-substituted-1,3-thiazol-5-yl)-2-alkoxybenzamides and 5-(2-N-(substituted aryl)-1,3-thiazol-5-yl)-2-alkoxy benzamides (8a-g) by reacting with n-alkylbromides (7a-b) in presence of a base. The newly synthesized compounds were characterized by IR, 1H-NMR and mass spectral data. Compounds were also screened for their antifungal activity.

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