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2,2-dimethyl 1-phenyl 3-(4-methoxyphenyl)-3,4-dihydronaphthalene-1,2,2(1H)-tricarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1608105-54-9 Structure
  • Basic information

    1. Product Name: 2,2-dimethyl 1-phenyl 3-(4-methoxyphenyl)-3,4-dihydronaphthalene-1,2,2(1H)-tricarboxylate
    2. Synonyms: 2,2-dimethyl 1-phenyl 3-(4-methoxyphenyl)-3,4-dihydronaphthalene-1,2,2(1H)-tricarboxylate
    3. CAS NO:1608105-54-9
    4. Molecular Formula:
    5. Molecular Weight: 474.51
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1608105-54-9.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: 2,2-dimethyl 1-phenyl 3-(4-methoxyphenyl)-3,4-dihydronaphthalene-1,2,2(1H)-tricarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethyl 1-phenyl 3-(4-methoxyphenyl)-3,4-dihydronaphthalene-1,2,2(1H)-tricarboxylate(1608105-54-9)
    11. EPA Substance Registry System: 2,2-dimethyl 1-phenyl 3-(4-methoxyphenyl)-3,4-dihydronaphthalene-1,2,2(1H)-tricarboxylate(1608105-54-9)
  • 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: 1608105-54-9(Hazardous Substances Data)

1608105-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608105-54-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,1,0 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1608105-54:
(9*1)+(8*6)+(7*0)+(6*8)+(5*1)+(4*0)+(3*5)+(2*5)+(1*4)=139
139 % 10 = 9
So 1608105-54-9 is a valid CAS Registry Number.

1608105-54-9Downstream Products

1608105-54-9Relevant articles and documents

Catalytic enantioselective C(sp3)H functionalization: Intramolecular benzylic [1,5]-hydride shift

Yu, Jie,Li, Nan,Chen, Dian-Feng,Luo, Shi-Wei

, p. 2859 - 2864 (2014)

The catalytic asymmetric [1,5]-hydride transfer/cyclization sequence involving benzylic C(sp3)H bond was established, providing tetrahydronaphthalene derivatives in moderate to high yield with up to 69% ee, by employing the copper complex of si

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