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13288-64-7

2-methyl-3,5-diphenyl-1,3-thiazolium-4-olate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13288-64-7 Structure

  • Basic information

    1. Product Name: 2-methyl-3,5-diphenyl-1,3-thiazolium-4-olate
    2. Synonyms: 2-methyl-3,5-diphenyl-1,3-thiazolium-4-olate
    3. CAS NO:13288-64-7
    4. Molecular Formula:
    5. Molecular Weight: 267.351
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13288-64-7.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-methyl-3,5-diphenyl-1,3-thiazolium-4-olate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-3,5-diphenyl-1,3-thiazolium-4-olate(13288-64-7)
    11. EPA Substance Registry System: 2-methyl-3,5-diphenyl-1,3-thiazolium-4-olate(13288-64-7)

  • 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: 13288-64-7(Hazardous Substances Data)

13288-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13288-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,8 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13288-64:
(7*1)+(6*3)+(5*2)+(4*8)+(3*8)+(2*6)+(1*4)=107
107 % 10 = 7
So 13288-64-7 is a valid CAS Registry Number.

13288-64-7Downstream Products

13288-64-7Relevant articles and documents

Reactivity of 2-methyl thioisomünchnone with acid chlorides

ávalos, Martín,Babiano, Reyes,Cintas, Pedro,Díaz, Jesús,Hursthouse, Michael B.,Jiménez, José L.,Light, Mark E.,López, Ignacio,Palacios, Juan C.

, p. 4657 - 4660 (2003)

This work describes the reactivity of 2-alkyl thioisomünchnones, exemplified here by the 2-methyl derivative, which behaves as nucleophile in the presence of both aliphatic and aromatic acid chlorides to give 2-heteroaryl ketones or 2-heteroaryl-1,3-diketones, respectively. However, 2-alkyl thioisomünchnones exhibit its characteristic 1,3-dipole behavior toward unsaturated systems.

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