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2-chloro-4-(2,4-dimethylphenyl)thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120413-99-2 Structure
  • Basic information

    1. Product Name: 2-chloro-4-(2,4-dimethylphenyl)thiophene
    2. Synonyms: 2-chloro-4-(2,4-dimethylphenyl)thiophene
    3. CAS NO:120413-99-2
    4. Molecular Formula:
    5. Molecular Weight: 222.738
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120413-99-2.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: 2-chloro-4-(2,4-dimethylphenyl)thiophene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-4-(2,4-dimethylphenyl)thiophene(120413-99-2)
    11. EPA Substance Registry System: 2-chloro-4-(2,4-dimethylphenyl)thiophene(120413-99-2)
  • 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: 120413-99-2(Hazardous Substances Data)

120413-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120413-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,1 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120413-99:
(8*1)+(7*2)+(6*0)+(5*4)+(4*1)+(3*3)+(2*9)+(1*9)=82
82 % 10 = 2
So 120413-99-2 is a valid CAS Registry Number.

120413-99-2Relevant articles and documents

A New and Simple Route to 3-Arylthiophenes

Sone, Tyo,Inoue, Manabu,Sato, Kazuaki

, p. 3779 - 3781 (1988)

3-Arylthiophenes were prepared from 2,5-dichlorothiophene in two steps. 2,5-Dichlorothiophene reacted regioselective with various aromatic compounds in the presence of AlCl3 under mild conditions to give 4-aryl-2-chlorothiophenes.The latter compounds were easily converted to the corresponding 3-arylthiophenes by catalytic dechloronation in good yields.

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