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CAS

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10522-05-1

Propionic acid 2-hydroxy-2-phenyl-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10522-05-1 Structure

  • Basic information

    1. Product Name: Propionic acid 2-hydroxy-2-phenyl-ethyl ester
    2. Synonyms: Propionic acid 2-hydroxy-2-phenyl-ethyl ester
    3. CAS NO:10522-05-1
    4. Molecular Formula:
    5. Molecular Weight: 194.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10522-05-1.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: Propionic acid 2-hydroxy-2-phenyl-ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propionic acid 2-hydroxy-2-phenyl-ethyl ester(10522-05-1)
    11. EPA Substance Registry System: Propionic acid 2-hydroxy-2-phenyl-ethyl ester(10522-05-1)

  • 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: 10522-05-1(Hazardous Substances Data)

10522-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10522-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10522-05:
(7*1)+(6*0)+(5*5)+(4*2)+(3*2)+(2*0)+(1*5)=51
51 % 10 = 1
So 10522-05-1 is a valid CAS Registry Number.

10522-05-1Downstream Products

10522-05-1Relevant articles and documents

Efficient and regioselective ring-opening of epoxides with carboxylic acid catalyzed by graphite oxide

Mirza-Aghayan, Maryam,Tavana, Mahdieh Molaee,Niazi, Elaheh Golam Alipour,Boukherroub, Rabah

, p. 532 - 538 (2020/07/17)

An efficient, simple and regioselective ring-opening reaction of epoxides with various carboxylic acids under metal-free conditions is reported. The ring-opening of epoxides takes place in the presence of graphite oxide as an efficient and available catalyst to produce the corresponding 2-hydroxy monoester and 1,2-diester derivatives in good yields. Regioselective attack of the nucleo-phile, short reaction times, metal-free conditions and reusability of catalyst are among the advantages of the present protocol.

PPL-CATALYZED RESOLUTION OF 1,2- AND 1,3-DIOLS IN METHYL PROPIONATE AS SOLVENT. AN APPLICATION OF THE TANDEM USE OF ENZYMES.

Janssen, A. J. M.,Klunder, A, J. H.,Zwanenburg, B.

, p. 7409 - 7416 (2007/10/02)

The Porcine Pancreatic Lipase (PPL)-catalyzed transesterification of 1-phenyl-1,2-ethanediol 1, 2-phenyl-1,2-propanediol 2, 1,2-decanediol 3, 1,2-pentanediol 4, 1,2-butanediol 5, 1,2-propanediol 6 and 1,3-butanediol 7 in methyl propionate as solvent was evaluated.In all substrates, the primary hydroxy group is esterified exclusively.The enantioselectivity displayed in this PPL-catalyzed reaction is moderate.The enantiomeric excess of diol (-)-1 is enhanced by subjecting propionate (-)-8, with a moderate ee (obtained by a PPL-catalyzed esterification of racemic 1 in methyl propionate), to an enzyme-catalyzed hydrolyis (tandem principle).

OXIDATION OF ISOXAZOLINES BY PERACIDS - A USEFUL ROUTE TO β-HYDROXY KETONES AND ACYLATED DIOLS

Park, Pyeong-uk,Kozikowski, Alan P.

, p. 6703 - 6706 (2007/10/02)

A method for bringing about the ring cleavage of isoxazolines by the use of peracids is described.

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