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1036713-42-4

2-chloro-6-(trifluoromethoxy)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1036713-42-4 Structure

  • Basic information

    1. Product Name: 2-chloro-6-(trifluoromethoxy)phenol
    2. Synonyms: 2-chloro-6-(trifluoromethoxy)phenol
    3. CAS NO:1036713-42-4
    4. Molecular Formula:
    5. Molecular Weight: 212.556
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036713-42-4.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: 2-chloro-6-(trifluoromethoxy)phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-6-(trifluoromethoxy)phenol(1036713-42-4)
    11. EPA Substance Registry System: 2-chloro-6-(trifluoromethoxy)phenol(1036713-42-4)

  • 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: 1036713-42-4(Hazardous Substances Data)

1036713-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036713-42-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,7,1 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1036713-42:
(9*1)+(8*0)+(7*3)+(6*6)+(5*7)+(4*1)+(3*3)+(2*4)+(1*2)=124
124 % 10 = 4
So 1036713-42-4 is a valid CAS Registry Number.

1036713-42-4Upstream product

1036713-42-4Downstream Products

1036713-42-4Relevant articles and documents

The trifluoromethoxy group as a fluorine twin in the Diels-Alder reactions of halogenated quinones

Magnier, Emmanuel,Diter, Patrick,Blazejewski, Jean-Claude

, p. 4575 - 4578 (2008)

We describe here a study devoted to the comparison of the relative influence of chlorine, fluorine, and trifluoromethoxy substituents on the regiochemical outcome of the Diels-Alder reaction. For this purpose, we examined the behavior of mixed 'halogenated' quinones bearing these groups in their cycloadditions with simple dienes. Contrary to the expectation based on its known electronic properties, the trifluoromethoxy group behaves very much more like a fluorine than a chlorine atom in such reactions. On the basis on an endo transition state demonstrated here for these additions, we tentatively suggest that non-bonded interactions are the main factor controlling the regiochemistry.

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