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1172608-32-0

C18H16BrF3O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1172608-32-0 Structure

  • Basic information

    1. Product Name: C18H16BrF3O2S
    2. Synonyms:
    3. CAS NO:1172608-32-0
    4. Molecular Formula:
    5. Molecular Weight: 433.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1172608-32-0.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: C18H16BrF3O2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H16BrF3O2S(1172608-32-0)
    11. EPA Substance Registry System: C18H16BrF3O2S(1172608-32-0)

  • 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: 1172608-32-0(Hazardous Substances Data)

1172608-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1172608-32-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,2,6,0 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1172608-32:
(9*1)+(8*1)+(7*7)+(6*2)+(5*6)+(4*0)+(3*8)+(2*3)+(1*2)=140
140 % 10 = 0
So 1172608-32-0 is a valid CAS Registry Number.

1172608-32-0Downstream Products

1172608-32-0Relevant articles and documents

Salts of Mosher's thioacid: agents for determining the enantiomer excess of SN2 substrates

Richman, Jack E.

supporting information; experimental part, p. 2793 - 2796 (2010/07/06)

The racemic and the (S)-enantiomer of Mosher's thioacid, 2-methoxy-2-trifluoromethylphenylacetic thioacid, form air-stable salts with Proton Sponge [1,8-bis(dimethylamino)naphthalene]. These salts are powerful nucleophiles that react cleanly (SN2 inversion) in CDCl3 with optically active alkyl halides ranging in reactivities from unactivated alkyl bromides and iodides to benzylic bromides. The diastereomeric excess (de) of the thioester products indicates the enantiomeric excess (ee) of the starting alkyl halides.

Thioacids and thioacid salts for determining the enantiomeric excess of chiral compounds containing an electrophilic carbon center

-

Page/Page column 14-15, (2010/07/02)

The invention provides novel chiral compounds including 2-methoxy-2-trifluoromethylphenylacetic thioacid useful to react with and analyze other chiral compounds that have an electrophilic chiral carbon center.

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