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2-Benzyl-5,5-dibromo-pent-4-enoic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126495-04-3 Structure
  • Basic information

    1. Product Name: 2-Benzyl-5,5-dibromo-pent-4-enoic acid tert-butyl ester
    2. Synonyms:
    3. CAS NO:126495-04-3
    4. Molecular Formula:
    5. Molecular Weight: 404.142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126495-04-3.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: 2-Benzyl-5,5-dibromo-pent-4-enoic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Benzyl-5,5-dibromo-pent-4-enoic acid tert-butyl ester(126495-04-3)
    11. EPA Substance Registry System: 2-Benzyl-5,5-dibromo-pent-4-enoic acid tert-butyl ester(126495-04-3)
  • 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: 126495-04-3(Hazardous Substances Data)

126495-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126495-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,9 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126495-04:
(8*1)+(7*2)+(6*6)+(5*4)+(4*9)+(3*5)+(2*0)+(1*4)=133
133 % 10 = 3
So 126495-04-3 is a valid CAS Registry Number.

126495-04-3Relevant articles and documents

A PRACTICAL PROCEDURE FOR THE CONVERSION OF ALDEHYDES TO TERMINAL ALKYNES BY A ONE CARBON HOMOLOGATION

Hijfte, Luc Van,Kolb, Michael,Witz, Pascale

, p. 3655 - 3656 (1989)

A convenient method for the conversion of aldehydes to terminal alkynes via the corresponding 1,1-dibromoalkenes is described.The key feature of the process is the use of megnesium in tetrahydrofuran for the debromination step.

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