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1-bromo-3,3,3-trichloro-1-phenyl-propene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35137-47-4 Structure
  • Basic information

    1. Product Name: 1-bromo-3,3,3-trichloro-1-phenyl-propene
    2. Synonyms: 1-bromo-3,3,3-trichloro-1-phenyl-propene
    3. CAS NO:35137-47-4
    4. Molecular Formula:
    5. Molecular Weight: 300.41
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35137-47-4.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-bromo-3,3,3-trichloro-1-phenyl-propene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-bromo-3,3,3-trichloro-1-phenyl-propene(35137-47-4)
    11. EPA Substance Registry System: 1-bromo-3,3,3-trichloro-1-phenyl-propene(35137-47-4)
  • 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: 35137-47-4(Hazardous Substances Data)

35137-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35137-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,3 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35137-47:
(7*3)+(6*5)+(5*1)+(4*3)+(3*7)+(2*4)+(1*7)=104
104 % 10 = 4
So 35137-47-4 is a valid CAS Registry Number.

35137-47-4Relevant articles and documents

In search of the spin-delocalization effect from the correlation analysis of relative rates of the trichloromethyl-bromo-addition reactions to fourteen p-Y-substituted phenylacetylenes

Jiang, Xi-Kui,Ji, Guo-Zhen,Xie, John Rong-Yuan

, p. 3017 - 3028 (1996)

A rigorous procedure was applied to the measurement of the relative rates, i.e. k(r)(Y) = k(Y)/k(H) of trichloromethyl-bromo-addition reactions to fourteen p-Y-substituted phenylacetylenes (I-Y, with Y = F, Cl, Br, Me, t-Bu, OMe, SMe, SiMe3, CF3, CN, NO2, SOMe, COMe, and CO2Me). The reaction was run in cyclohexane under nitrogen antmosphere at 65 ± 0.5°C. All products were derived from the intermediate YC6H4C = CHCCl3 adduct radicals. Correlation analysis of these rate data seems to suggest that both a polar and a spin-delocalization effect are operating at the transition state.

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