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CAS

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160549-09-7

(3S,4R,6R)-3-hexyl-4-hydroxy-6-undecyl-tetrahydropyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160549-09-7 Structure

  • Basic information

    1. Product Name: (3S,4R,6R)-3-hexyl-4-hydroxy-6-undecyl-tetrahydropyran-2-one
    2. Synonyms:
    3. CAS NO:160549-09-7
    4. Molecular Formula: C22H42O3
    5. Molecular Weight: 354.5671
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160549-09-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 483.15°C at 760 mmHg
    3. Flash Point: 183.676°C
    4. Appearance: N/A
    5. Density: 0.931g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.465
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3S,4R,6R)-3-hexyl-4-hydroxy-6-undecyl-tetrahydropyran-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3S,4R,6R)-3-hexyl-4-hydroxy-6-undecyl-tetrahydropyran-2-one(160549-09-7)
    12. EPA Substance Registry System: (3S,4R,6R)-3-hexyl-4-hydroxy-6-undecyl-tetrahydropyran-2-one(160549-09-7)

  • 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: 160549-09-7(Hazardous Substances Data)

160549-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160549-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,5,4 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 160549-09:
(8*1)+(7*6)+(6*0)+(5*5)+(4*4)+(3*9)+(2*0)+(1*9)=127
127 % 10 = 7
So 160549-09-7 is a valid CAS Registry Number.

160549-09-7Downstream Products

160549-09-7Relevant articles and documents

Enzymatic lactonization stategy for enantioselective synthesis of a tetrahydrolipstatin synthon

Sharma,Chattopadhyay

, p. 8059 - 8062 (2007/10/03)

A novel lipase-catalyzed protocol has been formulated for the simultaneous enantiocontrol of three stereogenic centers in a flexible acyclic system. This involved a porcine pancreatic lipase (PPL)-catalyzed δ- lactonization of a racemic 3,5-dihydroxy-2-alkyl ester to produce the lactone with high enantioselectivity (92.8%). The product lactone and its analogues are useful synthons for the asymmetric synthesis of various bioactive compounds, which include the potential anti-obesity compound, tetrahydrolipstatin.

Stereoselective syntheses of tetrahydroesterastin-β-lactam analogues

Huber,Schneider

, p. 1065 - 1076 (2007/10/02)

A total synthesis of the optically active tetrahydroesterastin-β-lactam analogue 2 using Miller's hydroxamate approach is described (Scheme 2). Significant modification of published procedures has resulted in a short and facile stereospecific preparation

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