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CAS

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476687-78-2

(E)-3-methyl-5-phenyl-2-pentene-1,5-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 476687-78-2 Structure

  • Basic information

    1. Product Name: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol
    2. Synonyms: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol
    3. CAS NO:476687-78-2
    4. Molecular Formula:
    5. Molecular Weight: 192.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 476687-78-2.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: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol(476687-78-2)
    11. EPA Substance Registry System: (E)-3-methyl-5-phenyl-2-pentene-1,5-diol(476687-78-2)

  • 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: 476687-78-2(Hazardous Substances Data)

476687-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 476687-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,6,8 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 476687-78:
(8*4)+(7*7)+(6*6)+(5*6)+(4*8)+(3*7)+(2*7)+(1*8)=222
222 % 10 = 2
So 476687-78-2 is a valid CAS Registry Number.

476687-78-2Relevant articles and documents

Diastereoselective construction of functionalized homoallylic alcohols by Ni-catalyzed diboron-promoted coupling of dienes and aldehydes

Hee, Yeon Cho,Morken, James P.

supporting information; experimental part, p. 16140 - 16141 (2009/05/08)

The nickel-catalyzed reaction of carbonyls and dienes was accomplished in a regio- and stereoselective fashion employing a stoichiometric amount of bis(pinacolato)diboron. This reductive coupling furnishes an allyl boronic ester as the reaction product, a compound which was readily converted to the derived allylic alcohol by oxidative workup. Copyright

Biocatalyzed preparation of the optically enriched stereoisomers of 4-methyl-2-phenyl-tetrahydro-2H-pyran (Doremox)

Brenna, Elisabetta,Fuganti, Claudio,Ronzani, Sabrina,Serra, Stefano

, p. 714 - 723 (2007/10/03)

The four stereoisomers of the rose oxide analogue Doremox were prepared in enantiomerically enriched form by enantiospecific bakers' yeast reduction of suitable derivatives and by lipase-mediated kinetic resolution of diol precursors.

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