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3854-53-3

2,2-Dimethyl-3-benzyl-buten-(3) is an organic compound characterized by its molecular formula C14H20. It features a buten-(3) backbone with a benzyl group attached to the third carbon, and two methyl groups on the second carbon. This structure contributes to its unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research. The compound's specific arrangement of atoms and functional groups may influence its reactivity and compatibility with other substances, making it a subject of interest for further study and development.

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  • 3854-53-3 Structure

  • Basic information

    1. Product Name: 2,2-Dimethyl-3-benzyl-buten-(3)
    2. Synonyms: 2,2-Dimethyl-3-benzyl-buten-(3)
    3. CAS NO:3854-53-3
    4. Molecular Formula:
    5. Molecular Weight: 174.286
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3854-53-3.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: 2,2-Dimethyl-3-benzyl-buten-(3)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-Dimethyl-3-benzyl-buten-(3)(3854-53-3)
    11. EPA Substance Registry System: 2,2-Dimethyl-3-benzyl-buten-(3)(3854-53-3)

  • 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: 3854-53-3(Hazardous Substances Data)

3854-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3854-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,5 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3854-53:
(6*3)+(5*8)+(4*5)+(3*4)+(2*5)+(1*3)=103
103 % 10 = 3
So 3854-53-3 is a valid CAS Registry Number.

3854-53-3Downstream Products

3854-53-3Relevant articles and documents

Alder-ene reaction of aryne with olefins

Chen, Zhao,Liang, Jinhua,Yin, Jun,Yu, Guang-Ao,Liu, Sheng Hua

supporting information, p. 5785 - 5787 (2013/10/01)

A novel intermolecular Alder-ene reaction based on aryne and olefins was developed. We performed this transformation under mild conditions such as at room temperature, and this reaction displayed high selectivity and good yields only in the presence of CsF. Hence, the intermolecular Alder-ene reaction of aryne with olefins provides an effective route to synthesize derivatives of olefins.

Palladium-catalyzed cross-coupling of aryl and alkenyl boronic acids with alkenes via oxidative addition of a carbon-boron bond to palladium(0)

Cho, Chan Sik,Uemura, Sakae

, p. 85 - 92 (2007/10/02)

Arylboronic acids react with alkenes in acetic acid at 25 deg C in the presence of a catalytic amount of palladium(II) acetate together with sodium acetate to give the corresponding aryl-substituted alkenes in high yields.Alkenylboronic acids react with alkenes under similar conditions to give the corresponding conjugated dienes stereospecifically, but the product yields are lower, compared with those from arylboronic acids.Similar treatment of sodium tetraphenylborate (NaBPh4) with alkenes also affords the corresponding phenylated alkenes in high yields together with biphenyl and benzene as side products.Oxidative addition of a carbon-boron bond to palladium(0), formed in situ, to give an organopalladium(II) species is assumed to be the key step of these cross-coupling reactions. Key words: Boronic acid; Aryl; Alkenyl; Alkene; Palladium; Oxidative addition

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