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(S)-2-Ethyl-tetrahydro-pyran-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82110-23-4 Structure
  • Basic information

    1. Product Name: (S)-2-Ethyl-tetrahydro-pyran-4-one
    2. Synonyms:
    3. CAS NO:82110-23-4
    4. Molecular Formula:
    5. Molecular Weight: 128.171
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82110-23-4.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)-2-Ethyl-tetrahydro-pyran-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-Ethyl-tetrahydro-pyran-4-one(82110-23-4)
    11. EPA Substance Registry System: (S)-2-Ethyl-tetrahydro-pyran-4-one(82110-23-4)
  • 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: 82110-23-4(Hazardous Substances Data)

82110-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82110-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,1 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82110-23:
(7*8)+(6*2)+(5*1)+(4*1)+(3*0)+(2*2)+(1*3)=84
84 % 10 = 4
So 82110-23-4 is a valid CAS Registry Number.

82110-23-4Downstream Products

82110-23-4Relevant articles and documents

Enzymes in Organic Synthesis. 25. Heterocyclic Ketones as Substrates of Horse Liver Alcohol Dehydrogenase. Highly Stereoselective Reductions of 2-Substituted Tetrahydropyran-4-ones

Haslegrave, J. Anthony,Jones, J. Bryan

, p. 4666 - 4671 (2007/10/02)

Horse liver alcohol dehydrogenase (HLADH) has been found to be an efficient catalyst for the reduction of O-heterocyclic ketones.Preparative-scale HLADH-catalyzed reductions of 2-substituted tetrahydropyran-4-ones are enantioselective, with reduction of e

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