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214626-49-0

2-Heptene-1,4-diol, 2-phenyl-, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214626-49-0 Structure

  • Basic information

    1. Product Name: 2-Heptene-1,4-diol, 2-phenyl-, (2Z)-
    2. Synonyms:
    3. CAS NO:214626-49-0
    4. Molecular Formula: C13H18O2
    5. Molecular Weight: 206.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214626-49-0.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: 2-Heptene-1,4-diol, 2-phenyl-, (2Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Heptene-1,4-diol, 2-phenyl-, (2Z)-(214626-49-0)
    11. EPA Substance Registry System: 2-Heptene-1,4-diol, 2-phenyl-, (2Z)-(214626-49-0)

  • 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: 214626-49-0(Hazardous Substances Data)

214626-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214626-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,6,2 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 214626-49:
(8*2)+(7*1)+(6*4)+(5*6)+(4*2)+(3*6)+(2*4)+(1*9)=120
120 % 10 = 0
So 214626-49-0 is a valid CAS Registry Number.

214626-49-0Downstream Products

214626-49-0Relevant articles and documents

Useful base promoted elaborations of oxiranyl ethers

Thurner, Angelika,Faigl, Ferenc,Toke, László,Mordini, Alessandro,Valacchi, Michela,Reginato, Gianna,Czira, Gábor

, p. 8173 - 8180 (2001)

Functionalized oxiranyl ethers can be regio- and stereoselectively converted into hydroxy oxetanes or cis-diols by treatment with organometallic bases. These two rearrangements can be conveniently carried out either using different reaction conditions sta

A new base promoted rearrangement of (E)-1-benzyloxy-2,3-epoxyalkanes

Thurner, Angelika,Faigl, Ferenc,Mordini, Alessandro,Bigi, Anna,Reginato, Gianna,Toeke, Laszlo

, p. 11597 - 11602 (1998)

(E)-1-benzyloxy-2,3-epoxyalkanes (4) underwent stereoselective rearrangement in the presence of LIDAKOR reagent and large excess of butyllithium producing (Z)-alkendiols (7) at ambident temperature. The same reaction serves anti oxetanes (6) at -75 °C whi

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