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1215180-93-0

diethyl (Z)-6-phenyl-2-hexen-4-yl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1215180-93-0 Structure

  • Basic information

    1. Product Name: diethyl (Z)-6-phenyl-2-hexen-4-yl phosphate
    2. Synonyms: diethyl (Z)-6-phenyl-2-hexen-4-yl phosphate
    3. CAS NO:1215180-93-0
    4. Molecular Formula:
    5. Molecular Weight: 312.346
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1215180-93-0.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: diethyl (Z)-6-phenyl-2-hexen-4-yl phosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diethyl (Z)-6-phenyl-2-hexen-4-yl phosphate(1215180-93-0)
    11. EPA Substance Registry System: diethyl (Z)-6-phenyl-2-hexen-4-yl phosphate(1215180-93-0)

  • 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: 1215180-93-0(Hazardous Substances Data)

1215180-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215180-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,5,1,8 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1215180-93:
(9*1)+(8*2)+(7*1)+(6*5)+(5*1)+(4*8)+(3*0)+(2*9)+(1*3)=120
120 % 10 = 0
So 1215180-93-0 is a valid CAS Registry Number.

1215180-93-0Relevant articles and documents

Copper-catalyzed γ-selective and stereospecific direct allylic alkylation of terminal alkynes: Synthesis of skipped enynes

Makida, Yusuke,Takayama, Yurie,Ohmiya, Hirohisa,Sawamura, Masaya

supporting information, p. 5350 - 5354 (2013/06/05)

Skipping out: The title reaction using internal secondary allylic phosphates proceeded with excellent γ regioselectivity and E stereoselectivity to give skipped enynes. Enantioenriched secondary allylic phosphates proceeded with 1,3-anti stereochemistry t

Copper-catalyzed γ-selective and stereospecific allylic alkylation of ketene silyl acetals

Li, Dong,Ohmiya, Hirohisa,Sawamura, Masaya

, p. 5672 - 5675 (2011/06/18)

Copper-catalyzed allylic alkylation of ketene silyl acetals proceeded with excellent γ-E-selectivity. Efficient α-to-γ chirality transfer with anti-selectivity occurred in the reaction of enantioenriched secondary allylic phosphates, affording enantioenri

Copper-catalyzed γ-selective and stereospecific allyl-aryl coupling between (Z)-acyclic and cyclic allylic phosphates and arylboronates

Ohmiya, Hirohisa,Yokokawa, Natsumi,Sawamura, Masaya

supporting information; experimental part, p. 2438 - 2440 (2010/07/10)

A Cu-catalyzed allyl-aryl coupling reaction between (Z)-acyclic or cyclic allylic phosphates and arylboronates proceeds with excellent γ-E-selectivity and 1,3-anti chirality transfer, which gives the corresponding coupling products with benzylic and allylic stereogenic centers. The wide availability and easy-to-handle nature of arylboronates, the inexpensiveness of the Cu catalyst system, and the high regio- and stereoselectivities are attractive features of this protocol.

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