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CAS

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109387-87-3

octan-5,7-dienoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109387-87-3 Structure

  • Basic information

    1. Product Name: octan-5,7-dienoic acid
    2. Synonyms: octan-5,7-dienoic acid
    3. CAS NO:109387-87-3
    4. Molecular Formula:
    5. Molecular Weight: 140.182
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109387-87-3.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: octan-5,7-dienoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: octan-5,7-dienoic acid(109387-87-3)
    11. EPA Substance Registry System: octan-5,7-dienoic acid(109387-87-3)

  • 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: 109387-87-3(Hazardous Substances Data)

109387-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109387-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 109387-87:
(8*1)+(7*0)+(6*9)+(5*3)+(4*8)+(3*7)+(2*8)+(1*7)=153
153 % 10 = 3
So 109387-87-3 is a valid CAS Registry Number.

109387-87-3Relevant articles and documents

Intramolecular tsujitrost-type allylation of carboxylic acids: Asymmetric synthesis of highly π-allyl donative lactones

Suzuki, Yusuke,Seki, Tomoaki,Tanaka, Shinji,Kitamura, Masato

, p. 9539 - 9542 (2015/08/24)

TsujiTrost-type asymmetric allylation of carboxylic acids has been realized by using a cationic CpRu complex with an axially chiral picolinic acid-type ligand (Cl-Naph-PyCOOH: naph = naphthyl, py = pyridine). The carboxylic acid and allylic alcohol intramolecularly condense by the liberation of water without stoichiometric activation of either nucleophile or electrophile part, thereby attaining high atom- and step-economy, and low E factor. This success can be ascribed to the higher reactivity of allylic alcohols as compared with the allyl ester products in soft Ru/hard Br?nstead acid combined catalysis, which can function under slightly acidic conditions unlike the traditional Pd-catalyzed system. Detailed analysis of the stereochemical outcome of the reaction using an enantiomerically enriched D-labeled substrate provides an intriguing view of enantioselection.

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