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CAS

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804519-82-2

3-Pentanone, 1-cyclohexyl-1-hydroxy-2-methyl-, (1S,2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 804519-82-2 Structure

  • Basic information

    1. Product Name: 3-Pentanone, 1-cyclohexyl-1-hydroxy-2-methyl-, (1S,2S)-
    2. Synonyms:
    3. CAS NO:804519-82-2
    4. Molecular Formula: C12H22O2
    5. Molecular Weight: 198.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 804519-82-2.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: 3-Pentanone, 1-cyclohexyl-1-hydroxy-2-methyl-, (1S,2S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Pentanone, 1-cyclohexyl-1-hydroxy-2-methyl-, (1S,2S)-(804519-82-2)
    11. EPA Substance Registry System: 3-Pentanone, 1-cyclohexyl-1-hydroxy-2-methyl-, (1S,2S)-(804519-82-2)

  • 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: 804519-82-2(Hazardous Substances Data)

804519-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 804519-82-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,5,1 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 804519-82:
(8*8)+(7*0)+(6*4)+(5*5)+(4*1)+(3*9)+(2*8)+(1*2)=162
162 % 10 = 2
So 804519-82-2 is a valid CAS Registry Number.

804519-82-2Downstream Products

804519-82-2Relevant articles and documents

Proline-catalyzed asymmetric aldol reactions of tetrahydro-4H-thiopyran-4- one with aldehydes

Ward, Dale E.,Jheengut, Vishal

, p. 8347 - 8350 (2007/10/03)

Proline-catalyzed enantioselective direct intermolecular aldol reactions of tetrahydro-4H-thiopyran-4-one with various aldehydes give anti adducts with high diastereo- and enantioselectivities in moderate to excellent yields. With the aromatic aldehydes b

HIGHLY ENANTIOSELECTIVE SYNTHESIS OF ANTI(THREO)-ALDOLS BY THE ASYMMETRIC ALDOL REACTION UTILIZING A CHIRAL AZAENOLATE

Narasaka, Koichi,Miwa, Tetsuo

, p. 1217 - 1220 (2007/10/02)

Diastereo- and enantioselective aldol reaction between 3-pentanone and aldehydes is achieved utilizing a chiral oxazolidine derived from 3-pentanone and chiral norephedrine.The reaction of a tin(II) azaenolate generated from the chiral oxazolidine with aldehydes affords predominantly anti(threo)-aldols of high enantiomeric purity.

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