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206194-02-7

(S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 206194-02-7 Structure

  • Basic information

    1. Product Name: (S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid
    2. Synonyms: (S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid
    3. CAS NO:206194-02-7
    4. Molecular Formula:
    5. Molecular Weight: 407.706
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 206194-02-7.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: (S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid(206194-02-7)
    11. EPA Substance Registry System: (S)-(-)-5-Chloro-2-methoxy-α-fluoro-α-[2-nitro-4-(trifluoromethyl)phenyl]benzeneacetic acid(206194-02-7)

  • 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: 206194-02-7(Hazardous Substances Data)

206194-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 206194-02-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,1,9 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 206194-02:
(8*2)+(7*0)+(6*6)+(5*1)+(4*9)+(3*4)+(2*0)+(1*2)=107
107 % 10 = 7
So 206194-02-7 is a valid CAS Registry Number.

206194-02-7Relevant articles and documents

PREPARATION OF 3-FLUORO OXINDOLE DERIVATIVES

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Page/Page column 12, (2010/02/11)

The present invention relates to novel itermediates of formula (1) wherein the wavy bond ( SIMILAR SIMILAR ) represents the racemate, the (R)-enantiomer or the (S)-enantiomer; and R is hydrogen, a carboxyl-protecting group or a cation of an addition salt;

The synthesis and characterization of BMS-204352 (MaxiPost) and related 3-fluorooxindoles as openers of maxi-K potassium channels

Hewawasam, Piyasena,Gribkoff, Valentin K.,Pendri, Yadagiri,Dworetzky, Steven I.,Meanwell, Nicholas A.,Martinez, Eduardo,Boissard, Christopher G.,Post-Munson, Debra J.,Trojnacki, Joanne T.,Yeleswaram, Krishnaswamy,Pajor, Lorraine M.,Knipe, Jay,Gao, Qi,Perrone, Robert,Starrett Jr., John E.

, p. 1023 - 1026 (2007/10/03)

3-Aryl-3-fluorooxindoles can be efficiently synthesized in two steps by the addition of an aryl Grignard to an isatin, followed by treatment with DAST. Oxindole 1 (BMS-204352; MaxiPost) can be isolated using chiral HPLC or prepared by employing chiral res

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