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108735-87-1

2-phenyl-4-formyl-thiazole oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108735-87-1 Structure

  • Basic information

    1. Product Name: 2-phenyl-4-formyl-thiazole oxime
    2. Synonyms: 2-phenyl-4-formyl-thiazole oxime
    3. CAS NO:108735-87-1
    4. Molecular Formula:
    5. Molecular Weight: 204.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108735-87-1.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: 2-phenyl-4-formyl-thiazole oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-4-formyl-thiazole oxime(108735-87-1)
    11. EPA Substance Registry System: 2-phenyl-4-formyl-thiazole oxime(108735-87-1)

  • 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: 108735-87-1(Hazardous Substances Data)

108735-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108735-87-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,3 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 108735-87:
(8*1)+(7*0)+(6*8)+(5*7)+(4*3)+(3*5)+(2*8)+(1*7)=141
141 % 10 = 1
So 108735-87-1 is a valid CAS Registry Number.

108735-87-1Relevant articles and documents

The effect of some 4,2 and 5,2 bisthiazole derivatives on nitro-oxidative stress and phagocytosis in acute experimental inflammation

Araniciu, Catalin,Parvu, Alina Elena,Palage, Mariana Doina,Oniga, Smaranda Dafina,Benedec, Daniela,Oniga, Ilioara,Oniga, Ovidiu

, p. 9240 - 9256 (2014/08/05)

Nineteen bisthiazoles were tested in order to assess their anti-inflammatory and antioxidant properties. First, we evaluated the in vitro direct antioxidant capacity of the bisthiazoles using the DPPH radical scavenging method. Then, the anti-inflammatory

Hantzsch reaction intermediates as a means to obtain bisthiazoles and 5-acetyl-bisthiazoles

Simiti,Oniga,Zaharia,Horn

, p. 794 - 796 (2007/10/03)

The synthesis, chemical and spectral data of some intermediates of Hantzsch's reaction is described. The synthesis of some 4-R-5-R1-2'-Aryl-2,4'-bisthiazoles was presented too. By interaction of acetic anhydride, hydroxythiasoline derivatives were converted to 5-acetyl-bisthiazoles.

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