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104367-32-0

(4-cyclohexylidenebut-3-en-1-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104367-32-0 Structure

  • Basic information

    1. Product Name: (4-cyclohexylidenebut-3-en-1-yl)benzene
    2. Synonyms: (4-cyclohexylidenebut-3-en-1-yl)benzene
    3. CAS NO:104367-32-0
    4. Molecular Formula:
    5. Molecular Weight: 212.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104367-32-0.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: (4-cyclohexylidenebut-3-en-1-yl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-cyclohexylidenebut-3-en-1-yl)benzene(104367-32-0)
    11. EPA Substance Registry System: (4-cyclohexylidenebut-3-en-1-yl)benzene(104367-32-0)

  • 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: 104367-32-0(Hazardous Substances Data)

104367-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104367-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104367-32:
(8*1)+(7*0)+(6*4)+(5*3)+(4*6)+(3*7)+(2*3)+(1*2)=100
100 % 10 = 0
So 104367-32-0 is a valid CAS Registry Number.

104367-32-0Downstream Products

104367-32-0Relevant articles and documents

Palladium(0)-catalyzed cross-coupling of 1,1-diboronates with vinyl bromides and 1,1-dibromoalkenes

Li, Huan,Zhang, Zhikun,Shangguan, Xianghang,Huang, Shan,Chen, Jun,Zhang, Yan,Wang, Jianbo

supporting information, p. 11921 - 11925 (2015/01/09)

Palladium-catalyzed cross-coupling reactions of 1,1-diboronates with vinyl bromides and dibromoalkenes were found to afford 1,4-dienes and allenes, respectively. These reactions utilize the high reactivities of both 1,1-diboronates and allylboron intermediates generated in the initial coupling.

Generation of allenic/propargylic zirconium complexes and subsequent cross-coupling reactions: A facile synthesis of multisubstituted allenes

Zhang, Hao,Fu, Xiaoping,Chen, Jingjin,Wang, Erjuan,Liu, Yuanhong,Li, Yuxue

supporting information; experimental part, p. 9351 - 9358 (2010/03/04)

(Chemical Equation Presented) The β-alkoxide elimination reaction of propargylic ether with Negishi reagent leads to allenes and/or alkynes after hydrolysis. The product distribution is highly dependent on the substitution pattern of starting propargylic

A new method for synthesis of allenes, including an optically active form, from aldehydes and alkenyl aryl sulfoxides by sulfoxide-metal exchange as the key reaction and an application to a total synthesis of male bean weevil sex attractant

Satoh, Tsuyoshi,Hanaki, Noriko,Kuramochi, Yuko,Inoue, Yujiro,Hosoya, Kayo,Sakai, Ken

, p. 2533 - 2549 (2007/10/03)

The sulfoxide-metal exchange reaction of β-acetoxy sulfoxides or β-mesyloxy sulfoxides, which were derived from alkenyl aryl sulfoxides and aldehydes in two steps, with a Grignard reagent or alkyllithium at low temperature gave allenes in good yields. Optically active allenes were synthesized starting from optically active 2-substituted ethenyl p-tolyl sulfoxides. A synthesis of (-)-methyl (E)-2,4,5-tetradecatrienoate, a male bean weevil sex attractant, was realized by this method.

THE REACTION OF β-PHENYLSULFINYL β,γ-UNSATURATED ETHERS WITH TRIBUTYLSTANNYLLITHIUM. A NEW ROUTE TO SUBSTITUTED ALLENES

Takeda, Takeshi,Suzuki, Koichi,Ohshima, Hiroyuki,Fujiwara, Tooru

, p. 1249 - 1250 (2007/10/02)

Substituted allenes were prepared in good yields by the reaction of β-phenylsulfinyl β,γ-unsaturated ethers with tributylstannyllithium.

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