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Benzonitrile, 2-[(4-fluorophenyl)methyl]-3,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144037-81-0 Structure
  • Basic information

    1. Product Name: Benzonitrile, 2-[(4-fluorophenyl)methyl]-3,6-dimethyl-
    2. Synonyms:
    3. CAS NO:144037-81-0
    4. Molecular Formula: C16H14FN
    5. Molecular Weight: 239.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144037-81-0.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: Benzonitrile, 2-[(4-fluorophenyl)methyl]-3,6-dimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzonitrile, 2-[(4-fluorophenyl)methyl]-3,6-dimethyl-(144037-81-0)
    11. EPA Substance Registry System: Benzonitrile, 2-[(4-fluorophenyl)methyl]-3,6-dimethyl-(144037-81-0)
  • 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: 144037-81-0(Hazardous Substances Data)

144037-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144037-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,3 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 144037-81:
(8*1)+(7*4)+(6*4)+(5*0)+(4*3)+(3*7)+(2*8)+(1*1)=110
110 % 10 = 0
So 144037-81-0 is a valid CAS Registry Number.

144037-81-0Downstream Products

144037-81-0Relevant articles and documents

Synthesis of poly(methylphenyl)acetonitriles by the aryne reaction

Waggenspack,Tran,Taylor,Yeung,Morgan,Deshmukh,Khanapure,Biehl

, p. 765 - 768 (2007/10/02)

Several 2-(arylmethyl) derivatives of 3,6-dimethyl- and 3,4,5,6-tetramethylbenzonitriles have been prepared in good yields most likely by a tandem addition-rearrangement reaction of the appropriate bromoarene and arylacetonitrile under aryne-forming conditions. Additionally, several 2-aryl-2-(1,4-dimethyl-2-naphthyl)acetonitriles were obtained by the usual aryne mechanism from the reaction of 2-bromo-1,4-dimethylnaphthalene and arylacetonitriles with lithium tetramethylpiperidide.

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