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CAS

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72449-22-0

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

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  • 72449-22-0 Structure

  • Basic information

    1. Product Name: (2SR,3SR)-1-cyclohexyl-3-hydroxy-2-methyl-3-phenylpropan-1-one
    2. Synonyms:
    3. CAS NO:72449-22-0
    4. Molecular Formula:
    5. Molecular Weight: 246.349
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72449-22-0.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: (2SR,3SR)-1-cyclohexyl-3-hydroxy-2-methyl-3-phenylpropan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2SR,3SR)-1-cyclohexyl-3-hydroxy-2-methyl-3-phenylpropan-1-one(72449-22-0)
    11. EPA Substance Registry System: (2SR,3SR)-1-cyclohexyl-3-hydroxy-2-methyl-3-phenylpropan-1-one(72449-22-0)

  • 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: 72449-22-0(Hazardous Substances Data)

72449-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72449-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,4 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72449-22:
(7*7)+(6*2)+(5*4)+(4*4)+(3*9)+(2*2)+(1*2)=130
130 % 10 = 0
So 72449-22-0 is a valid CAS Registry Number.

72449-22-0Downstream Products

72449-22-0Relevant articles and documents

Titanium tetraiodide-promoted reductive enolate formation of α-tosyloxy ketone derivatives and aldol reaction with aldehydes

Hachiya, Iwao,Inagaki, Takao,Ishihara, Yasuhisa,Shimizu, Makoto

, p. 419 - 421 (2011)

Titanium tetraiodide-promoted reductive enolate formation from α-tosyloxy ketone derivatives and subsequent aldol reaction of the resulting enolates with aldehydes gave β-hydroxy ketones.

Enolboration. 5. An Examination of the Effects of Amine, Solvent, and Other Reaction Parameters on the Stereoselective Enolboration of Ketones with Various Chx2BX Reagents. An Optimized Procedure To Achieve the Stereoselective Synthesis of E Enol Borinate

Ganesan, Kumeraperumal,Brown, Herbert C.

, p. 7162 - 7169 (2007/10/02)

The effects of amine, solvent, concentration, temperature and other reaction parameters in controlling the enolate geometry have been systematically investigated in the present study.A 11B NMR study of the interaction of representative tertiary amines of

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