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133392-22-0

(2S)-2-hydroxy-2-(2-hydroxy-5-methoxyphenyl)ethanoic acid (-)-menthyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133392-22-0 Structure

  • Basic information

    1. Product Name: (2S)-2-hydroxy-2-(2-hydroxy-5-methoxyphenyl)ethanoic acid (-)-menthyl ester
    2. Synonyms: (2S)-2-hydroxy-2-(2-hydroxy-5-methoxyphenyl)ethanoic acid (-)-menthyl ester
    3. CAS NO:133392-22-0
    4. Molecular Formula:
    5. Molecular Weight: 336.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133392-22-0.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: (2S)-2-hydroxy-2-(2-hydroxy-5-methoxyphenyl)ethanoic acid (-)-menthyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S)-2-hydroxy-2-(2-hydroxy-5-methoxyphenyl)ethanoic acid (-)-menthyl ester(133392-22-0)
    11. EPA Substance Registry System: (2S)-2-hydroxy-2-(2-hydroxy-5-methoxyphenyl)ethanoic acid (-)-menthyl ester(133392-22-0)

  • 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: 133392-22-0(Hazardous Substances Data)

133392-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133392-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,9 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133392-22:
(8*1)+(7*3)+(6*3)+(5*3)+(4*9)+(3*2)+(2*2)+(1*2)=110
110 % 10 = 0
So 133392-22-0 is a valid CAS Registry Number.

133392-22-0Downstream Products

133392-22-0Relevant articles and documents

HIGHLY REGIO- AND DIASTEREOSELECTIVE FRIEDEL-CRAFTS ALKYLATION OF PHENOLS. SYNTHESIS OF 2-HYDROXYMANDELIC ESTERS

Bigi, F.,Casnati, G.,Sartori, G.,Dalprato, C.,Bortolini, R.

, p. 861 - 864 (1990)

Ortho-hydroxyalkylation of phenol substrates was performed via coordinative complexes of metal phenolates with chiral glyoxylates: optically active 2-hydroxymandelic esters have been obtained with good yields and very high diastereoselectivity (up to 94pe

Stereoselective Synthesis of Optically Active 2-Hydroxymandelic Acids and Esters via Friedel-Crafts Coordinated Reaction: Crystal Structure of Chiral Dichloro[2-(1-oxido-1-menthoxycarbonylmethyl)-4-methoxyphenoxido-O,O,O] titanium?

Bigi, Franca,Bocelli, Gabriele,Maggi, Raimondo,Sartori, Giovanni

, p. 5004 - 5009 (2007/10/03)

Highly diastereoselective hydroxyalkylation of phenols with chiral glyoxylates was performed. Hydrolysis or reduction of the esters 3 afforded 2-hydroxymandelic acids 6 and diols 5 in high yields and enantiomeric pure form. Mechanistic evidence of chelati

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