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105087-06-7

(S)-(E)-oct-3-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105087-06-7 Structure

  • Basic information

    1. Product Name: (S)-(E)-oct-3-en-2-ol
    2. Synonyms: (S)-(E)-oct-3-en-2-ol
    3. CAS NO:105087-06-7
    4. Molecular Formula:
    5. Molecular Weight: 128.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105087-06-7.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: (S)-(E)-oct-3-en-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(E)-oct-3-en-2-ol(105087-06-7)
    11. EPA Substance Registry System: (S)-(E)-oct-3-en-2-ol(105087-06-7)

  • 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: 105087-06-7(Hazardous Substances Data)

105087-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105087-06-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,8 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105087-06:
(8*1)+(7*0)+(6*5)+(5*0)+(4*8)+(3*7)+(2*0)+(1*6)=97
97 % 10 = 7
So 105087-06-7 is a valid CAS Registry Number.

105087-06-7Upstream product

105087-06-7Relevant articles and documents

Biocatalytic Enantioselective Oxidation of Sec-Allylic Alcohols with Flavin-Dependent Oxidases

Gandomkar, Somayyeh,Jost, Etta,Loidolt, Doris,Swoboda, Alexander,Pickl, Mathias,Elaily, Wael,Daniel, Bastian,Fraaije, Marco W.,Macheroux, Peter,Kroutil, Wolfgang

, p. 5264 - 5271 (2019)

The oxidation of allylic alcohols is challenging to perform in a chemo- as well as stereo-selective fashion at the expense of molecular oxygen using conventional chemical protocols. Here, we report the identification of a library of flavin-dependent oxidases including variants of the berberine bridge enzyme (BBE) analogue from Arabidopsis thaliana (AtBBE15) and the 5-(hydroxymethyl)furfural oxidase (HMFO) and its variants (V465T, V465S, V465T/W466H and V367R/W466F) for the enantioselective oxidation of sec-allylic alcohols. While primary and benzylic alcohols as well as certain sugars are well known to be transformed by flavin-dependent oxidases, sec-allylic alcohols have not been studied yet except in a single report. The model substrates investigated were oxidized enantioselectively in a kinetic resolution with an E-value of up to >200. For instance HMFO V465S/T oxidized the (S)-enantiomer of (E)-oct-3-en-2-ol (1 a) and (E)-4-phenylbut-3-en-2-ol with E>200 giving the remaining (R)-alcohol with ee>99% at 50% conversion. The enantioselectivity could be decreased if required by medium engineering by the addition of cosolvents (e. g. dimethyl sulfoxide).

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