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CAS

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29246-94-4

(S)-3,3,3-trifluoro-2-hydroxy-2-phenylpropanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29246-94-4 Structure

  • Basic information

    1. Product Name: (S)-3,3,3-trifluoro-2-hydroxy-2-phenylpropanoic acid
    2. Synonyms: (S)-3,3,3-trifluoro-2-hydroxy-2-phenylpropanoic acid
    3. CAS NO:29246-94-4
    4. Molecular Formula:
    5. Molecular Weight: 220.148
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29246-94-4.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: (S)-3,3,3-trifluoro-2-hydroxy-2-phenylpropanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3,3,3-trifluoro-2-hydroxy-2-phenylpropanoic acid(29246-94-4)
    11. EPA Substance Registry System: (S)-3,3,3-trifluoro-2-hydroxy-2-phenylpropanoic acid(29246-94-4)

  • 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: 29246-94-4(Hazardous Substances Data)

29246-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29246-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,4 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29246-94:
(7*2)+(6*9)+(5*2)+(4*4)+(3*6)+(2*9)+(1*4)=134
134 % 10 = 4
So 29246-94-4 is a valid CAS Registry Number.

29246-94-4Relevant articles and documents

Asymmetric organozincate additions to ethyl 2,2,2-trifluoropyruvate

Gosselin, Francis,Britton, Robert A.,Mowat, Jeffrey,O'Shea, Paul D.,Davies, Ian W.

, p. 2193 - 2196 (2007)

A chromatography-free synthesis of enantiomerically enriched chiral α-trifluoromethyl α-hydroxy acids prepared via an asymmetric (R)-BINOL-mediated organozincate addition to ethyl 2,2,2-trifluoropyruvate (1) is reported. Georg Thieme Verlag Stuttgart.

An efficient method for the preparation of Chiral Mosher's acid analogues

Kawano, Yoshikazu,Kaneko, Nobuya,Mukaiyama, Teruaki

, p. 304 - 305 (2007/10/03)

A diastereoselective trifluoromethylation of chiral α-keto esters derived from isosorbide with TMSCF3 in the presence of a Lewis-base catalyst gave the corresponding trifluoromethylated α-hydroxy esters in good yields with moderate to high dias

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