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1-acetoxy-4-(4-chloro-butoxy)-butane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55847-35-3 Structure
  • Basic information

    1. Product Name: 1-acetoxy-4-(4-chloro-butoxy)-butane
    2. Synonyms: 1-acetoxy-4-(4-chloro-butoxy)-butane
    3. CAS NO:55847-35-3
    4. Molecular Formula:
    5. Molecular Weight: 222.712
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55847-35-3.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-acetoxy-4-(4-chloro-butoxy)-butane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-acetoxy-4-(4-chloro-butoxy)-butane(55847-35-3)
    11. EPA Substance Registry System: 1-acetoxy-4-(4-chloro-butoxy)-butane(55847-35-3)
  • 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: 55847-35-3(Hazardous Substances Data)

55847-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55847-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,4 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55847-35:
(7*5)+(6*5)+(5*8)+(4*4)+(3*7)+(2*3)+(1*5)=153
153 % 10 = 3
So 55847-35-3 is a valid CAS Registry Number.

55847-35-3Downstream Products

55847-35-3Relevant articles and documents

Bi(III) halides as efficient catalysts for the O-acylative cleavage of tetrahydrofurans: An expeditious entry to tetralins

Coles, Simon J.,Costello, James F.,Draffin, William N.,Hursthouse, Michael B.,Paver, Simon P.

, p. 4447 - 4452 (2005)

The mild (DCM/20°C), quantitative, regioselective, O-acylative cleavage of tetrahydrofurans using organic acid halides with catalytic Bi(III) halides is reported. X-ray crystallography is used to rationalise the failure of the reaction in the case of certain crowded acid chlorides, and a useful aspect of chemoselectivity is revealed. The synthetic potential of this reaction is illustrated with a highly efficient O-acylative cleavage/intramolecular alkylation approach to tetralins.

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