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1033265-74-5

(Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • (Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile

    Cas No: 1033265-74-5

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  • 1033265-74-5 Structure

  • Basic information

    1. Product Name: (Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile
    2. Synonyms: (Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile
    3. CAS NO:1033265-74-5
    4. Molecular Formula:
    5. Molecular Weight: 274.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1033265-74-5.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: (Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile(1033265-74-5)
    11. EPA Substance Registry System: (Z)-2-hexylidene-2-(5-methoxy-2-nitrophenyl)acetonitrile(1033265-74-5)

  • 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: 1033265-74-5(Hazardous Substances Data)

1033265-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1033265-74-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,3,2,6 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1033265-74:
(9*1)+(8*0)+(7*3)+(6*3)+(5*2)+(4*6)+(3*5)+(2*7)+(1*4)=115
115 % 10 = 5
So 1033265-74-5 is a valid CAS Registry Number.

1033265-74-5Downstream Products

1033265-74-5Relevant articles and documents

Palladium-catalyzed synthesis of 3-indolecarboxylic acid derivatives

Soederberg, Bjoern C. G.,Banini, Serge R.,Turner, Michael R.,Minter, Aaron R.,Arrington, Amanda K.

, p. 903 - 912 (2008)

Indoles having an ester functionality in the 3-position were prepared from 2-(2-nitrophenyl)propenoic acid derivatives via a palladium-catalyzed reductive N-heteroannulation using carbon monoxide as the ultimate reducing agent. The starting materials were

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