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514213-33-3

Cyclopentanone, 2,3-dihydroxy-2-methoxy-3-methyl-, (3S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 514213-33-3 Structure

  • Basic information

    1. Product Name: Cyclopentanone, 2,3-dihydroxy-2-methoxy-3-methyl-, (3S)- (9CI)
    2. Synonyms: Cyclopentanone, 2,3-dihydroxy-2-methoxy-3-methyl-, (3S)- (9CI)
    3. CAS NO:514213-33-3
    4. Molecular Formula: C7H12O4
    5. Molecular Weight: 160.16778
    6. EINECS: N/A
    7. Product Categories: METHOXY;ALCOHOL;CYCLOPENTANE
    8. Mol File: 514213-33-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 258.5±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.27±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 10.67±0.40(Predicted)
    10. CAS DataBase Reference: Cyclopentanone, 2,3-dihydroxy-2-methoxy-3-methyl-, (3S)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Cyclopentanone, 2,3-dihydroxy-2-methoxy-3-methyl-, (3S)- (9CI)(514213-33-3)
    12. EPA Substance Registry System: Cyclopentanone, 2,3-dihydroxy-2-methoxy-3-methyl-, (3S)- (9CI)(514213-33-3)

  • 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: 514213-33-3(Hazardous Substances Data)

514213-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 514213-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,4,2,1 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 514213-33:
(8*5)+(7*1)+(6*4)+(5*2)+(4*1)+(3*3)+(2*3)+(1*3)=103
103 % 10 = 3
So 514213-33-3 is a valid CAS Registry Number.

514213-33-3Relevant articles and documents

Asymmetric oxidation of 3-alkyl-1,2-cyclopentanediones. Part 1: 3-Hydroxylation of 3-alkyl-1,2-cyclopentanediones

Paju, Anne,Kanger, Tonis,Pehk, Tonis,Mueuerisepp, Aleksander-Mati,Lopp, Margus

, p. 2439 - 2448 (2007/10/03)

3-Alkyl-1,2-cyclopentanediones undergo asymmetric 3-hydroxylation with the Sharpless Ti-complex resulting in enantiomeric 3-hydroxy carbonyl compounds with ee up to 95% in yields of 22-40%.

Asymmetric oxidation of 1,2-cyclopentanediones

Paju, Anne,Kanger, T?nis,Pehk, T?nis,Lopp, Margus

, p. 6883 - 6887 (2007/10/03)

Cyclic 3-alkyl-1,2-cyclopentanediones undergo a direct asymmetric oxidation with the DET/Ti(OiPr)4/ tBuOOH oxidative system, resulting in enantiomeric α-hydroxy compounds and ring-cleaved hydroxylated acids (lactones) up to 95% ee. (C) 2000 Elsevier Science Ltd.

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