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107686-16-8

4-phenyl-6-heptene-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107686-16-8 Structure

  • Basic information

    1. Product Name: 4-phenyl-6-heptene-1-ol
    2. Synonyms: 4-phenyl-6-heptene-1-ol
    3. CAS NO:107686-16-8
    4. Molecular Formula:
    5. Molecular Weight: 190.285
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107686-16-8.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: 4-phenyl-6-heptene-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-phenyl-6-heptene-1-ol(107686-16-8)
    11. EPA Substance Registry System: 4-phenyl-6-heptene-1-ol(107686-16-8)

  • 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: 107686-16-8(Hazardous Substances Data)

107686-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107686-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107686-16:
(8*1)+(7*0)+(6*7)+(5*6)+(4*8)+(3*6)+(2*1)+(1*6)=138
138 % 10 = 8
So 107686-16-8 is a valid CAS Registry Number.

107686-16-8Downstream Products

107686-16-8Relevant articles and documents

Iron-catalyzed ring-opening azidation and allylation of O-heterocycles

Sawama, Yoshinari,Shibata, Kyoshiro,Sawama, Yuka,Takubo, Masato,Monguchi, Yasunari,Krause, Norbert,Sajiki, Hironao

, p. 5282 - 5285 (2013)

We have established the first catalytic C-C and C-N bond formation reactions of O-heterocycles (e.g., tetrahydrofuran, phthalane, and lactone derivatives) using iron trichloride as a catalyst in the presence of TMSN 3 or allylsilanes accompanie

Direct substitution of the hydroxy group in alcohols with silyl nucleophiles catalyzed by indium trichloride

Yasuda, Makoto,Saito, Takahiro,Ueba, Masako,Baba, Akio

, p. 1414 - 1416 (2007/10/03)

Straightforward substitution: An excellent combination of a silyl nucleophile and indium catalyst was used to accomplish the dehydroxylation/ alkylation of alcohols under nearly neutral conditions (see scheme, Si = silyl group) even though this type of reaction usually requires at least an equimolar amount of acid.

Regioselective Ring-Cleavage Reaction of Tetrahydrofurans and Tetrahydropyrans Accompanied by Carbon-Carbon Bond Formation

Oku, Akira,Homoto, Yukio,Harada, Toshiro

, p. 1495 - 1498 (2007/10/02)

Various 2-substituted tetrahydrofurans and tetrahydropyrans were cleaved regioselectively accompanied by a simultaneous carbon-carbon bond formation at the highly substituted α carbon atom by using the reagent system of titanium tetrachloride and allyl- (

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