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36143-65-4

[S,(+)]-2,3-Decadienoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 36143-65-4 Structure

  • Basic information

    1. Product Name: [S,(+)]-2,3-Decadienoic acid
    2. Synonyms: [S,(+)]-2,3-Decadienoic acid
    3. CAS NO:36143-65-4
    4. Molecular Formula:
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 36143-65-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [S,(+)]-2,3-Decadienoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: [S,(+)]-2,3-Decadienoic acid(36143-65-4)
    11. EPA Substance Registry System: [S,(+)]-2,3-Decadienoic acid(36143-65-4)

  • 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: 36143-65-4(Hazardous Substances Data)

36143-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36143-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36143-65:
(7*3)+(6*6)+(5*1)+(4*4)+(3*3)+(2*6)+(1*5)=104
104 % 10 = 4
So 36143-65-4 is a valid CAS Registry Number.

36143-65-4Downstream Products

36143-65-4Relevant articles and documents

Stereochemical Course of an Enzyme-Catalyzed Allene-Acetylene Isomerization

Schwab, John M.,Lin, Daniel C. T.

, p. 6046 - 6052 (2007/10/02)

An allene-acetylene isomerase (AAI) isolated from hog liver interconverts the N-acetylcysteamine thio ester of 3-decynoic acid (3-decynoyl-NAC) and (+)-2,3-decadienoyl-NAC.It is thus far the only enzyme that has been isolated that produces (or utilizes) an allenic compound and that is not inactivated by that same allene.Although physical and kinetic characteristics of the enzyme have previously been obtained, details of its mechanism of action remain unknown.The stereochemical course of the AAI-catalyzed propalgylic rearrangement has now been determined, by synthesis of 2,3-- and 2,3- decadienoyl-NAC and enzymatic conversion of these substrates to 3-1>decanoyl-NAC.Derivatization of the chirality labeled acetylenes, followed by 2H NMR analysis, has shown that protonation occurs on the si face at C-2 of the allene.X-ray crystallographic analysis of a derivative has revealed that (+)-2,3-decadienoic acid possesses the S configuration.The enzyme-mediated propargylic rearrangement is therefore a suprafacial process, apparently involving a single active-site base.

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