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1-(1-Bromo-but-3-enyl)-3-methoxy-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134619-73-1 Structure
  • Basic information

    1. Product Name: 1-(1-Bromo-but-3-enyl)-3-methoxy-benzene
    2. Synonyms: 1-(1-Bromo-but-3-enyl)-3-methoxy-benzene
    3. CAS NO:134619-73-1
    4. Molecular Formula:
    5. Molecular Weight: 241.128
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134619-73-1.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: 1-(1-Bromo-but-3-enyl)-3-methoxy-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1-Bromo-but-3-enyl)-3-methoxy-benzene(134619-73-1)
    11. EPA Substance Registry System: 1-(1-Bromo-but-3-enyl)-3-methoxy-benzene(134619-73-1)
  • 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: 134619-73-1(Hazardous Substances Data)

134619-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134619-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,1 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134619-73:
(8*1)+(7*3)+(6*4)+(5*6)+(4*1)+(3*9)+(2*7)+(1*3)=131
131 % 10 = 1
So 134619-73-1 is a valid CAS Registry Number.

134619-73-1Downstream Products

134619-73-1Relevant articles and documents

Halogenative Allylation and Reduction of Aromatic Acetals by Double Substitution of Alkoxyl Groups in Acetal

Oriyama, Takeshi,Iwanami, Katsuyuki,Tsukamoto, Kazuhisa,Ichimura, Yuichi,Koga, Gen

, p. 1410 - 1412 (1991)

In the presence of excessive amount of acetyl halide along with a catalytic amount of tin(II) halide, aromatic acetals react with allyltrimethylsilane or triethylsilane to give α-allylbenzyl halides or benzyl halides, respectively, in good to excellent yields.

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