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578763-81-2

1-Propanol,3-(1-cyclohexen-1-yloxy)-2-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 578763-81-2 Structure

  • Basic information

    1. Product Name: 1-Propanol,3-(1-cyclohexen-1-yloxy)-2-methyl-(9CI)
    2. Synonyms: 1-Propanol,3-(1-cyclohexen-1-yloxy)-2-methyl-(9CI)
    3. CAS NO:578763-81-2
    4. Molecular Formula: C10H18O2
    5. Molecular Weight: 170.24872
    6. EINECS: N/A
    7. Product Categories: METHOXY
    8. Mol File: 578763-81-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Propanol,3-(1-cyclohexen-1-yloxy)-2-methyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Propanol,3-(1-cyclohexen-1-yloxy)-2-methyl-(9CI)(578763-81-2)
    11. EPA Substance Registry System: 1-Propanol,3-(1-cyclohexen-1-yloxy)-2-methyl-(9CI)(578763-81-2)

  • 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: 578763-81-2(Hazardous Substances Data)

578763-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 578763-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,8,7,6 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 578763-81:
(8*5)+(7*7)+(6*8)+(5*7)+(4*6)+(3*3)+(2*8)+(1*1)=222
222 % 10 = 2
So 578763-81-2 is a valid CAS Registry Number.

578763-81-2Relevant articles and documents

Chiral and flexible 2,4-pentanediol-tethered cyclopropanation of olefins with a carbenoid derived from a diazo ester to construct three stereogenic centers

Sugimura, Takashi,Mori, Atsushi,Tai, Akira,Tei, Takahiro,Sakamoto, Yasuhiro,Okuyama, Tadashi

, p. 881 - 890 (2007/10/03)

2,4-Pentanediol-tethered cyclopropanation of an olefin with an internal carbenoid generated from a diazo ester proceeded smoothly to give a chiral adduct having three stereogenic centers under full stereocontrol. The high stereoselectivity was not affected by the structure of the olefinic portion, studied so far with six substrates. Conversion of the product cyclopropane to other optically active compounds is also reported.

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