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CAS

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76613-04-2

1,4-dimethyl-1,4-dihydrobiphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76613-04-2 Structure

  • Basic information

    1. Product Name: 1,4-dimethyl-1,4-dihydrobiphenyl
    2. Synonyms:
    3. CAS NO:76613-04-2
    4. Molecular Formula:
    5. Molecular Weight: 184.281
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76613-04-2.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: 1,4-dimethyl-1,4-dihydrobiphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-dimethyl-1,4-dihydrobiphenyl(76613-04-2)
    11. EPA Substance Registry System: 1,4-dimethyl-1,4-dihydrobiphenyl(76613-04-2)

  • 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: 76613-04-2(Hazardous Substances Data)

76613-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76613-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,1 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76613-04:
(7*7)+(6*6)+(5*6)+(4*1)+(3*3)+(2*0)+(1*4)=132
132 % 10 = 2
So 76613-04-2 is a valid CAS Registry Number.

76613-04-2Downstream Products

76613-04-2Relevant articles and documents

Metal-Ammonia Reduction: Effect of Methyl Substituents and a Question Concerning Protonation Sites in Dianions

Rabideau, Peter W.,Peters, N. Kent,Huser, Diane L.

, p. 1593 - 1597 (1981)

The effect of substituents on Birch reductions and other metal-ammonia processes has received considerable attention.Since the intermediate(s) is negatively charged, activation and orientation effects have been dealt with in terms of electron donation or withdrawal of substituents.The methyl group displays somewhat irregular behavior in naphthalenes and biphenyls, and an explanation is offered in terms of methyl location on a charge-bearing or non-charge-bearing carbon in the intermediates.The observation is also made that protonation of dianions (produced by electron addition) always seems to lead to the most stable monoanion.Reasons for this are discussed.

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