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cyclohex-2-en-1-yl isobutyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76475-04-2 Structure
  • Basic information

    1. Product Name: cyclohex-2-en-1-yl isobutyrate
    2. Synonyms: cyclohex-2-en-1-yl isobutyrate
    3. CAS NO:76475-04-2
    4. Molecular Formula:
    5. Molecular Weight: 168.236
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76475-04-2.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: cyclohex-2-en-1-yl isobutyrate(CAS DataBase Reference)
    10. NIST Chemistry Reference: cyclohex-2-en-1-yl isobutyrate(76475-04-2)
    11. EPA Substance Registry System: cyclohex-2-en-1-yl isobutyrate(76475-04-2)
  • 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: 76475-04-2(Hazardous Substances Data)

76475-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76475-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,7 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76475-04:
(7*7)+(6*6)+(5*4)+(4*7)+(3*5)+(2*0)+(1*4)=152
152 % 10 = 2
So 76475-04-2 is a valid CAS Registry Number.

76475-04-2Downstream Products

76475-04-2Relevant articles and documents

Catalytic Electrophilic Alkylation of p-Quinones through a Redox Chain Reaction

Xu, Xiao-Long,Li, Zhi

supporting information, p. 8196 - 8200 (2017/06/30)

Allylation and benzylation of p-quinones was achieved through an unusual redox chain reaction. Mechanistic studies suggest that the existence of trace hydroquinone initiates a redox chain reaction that consists of a Lewis acid catalyzed Friedel–Crafts alkylation and a subsequent redox equilibrium that regenerates hydroquinone. The electrophiles could be various allylic and benzylic esters. The addition of Hantzsch ester as an initiator improves the efficiency of the reaction.

Indium-mediated Reformatsky-Claisen rearrangement

Ishihara, Jun,Watanabe, Yuki,Koyama, Noriko,Nishino, Yukihiro,Takahashi, Keisuke,Hatakeyama, Susumi

experimental part, p. 3659 - 3667 (2011/06/21)

A new variant of the Reformatsky-Claisen rearrangement is described. The reaction of substituted allyl α-bromoacetates with indium and indium(III) chloride under ultrasonication provides a general entry into the functionalized synthon.

Reactions du n=chloroparatoluenesulfonamidate de sodium (chloramine t) sur les olefines en miliu acide organique

Damin, Bernard,Garapon, Jacques,Sillion, Bernard

, p. 1709 - 1710 (2007/10/02)

Vic. chloro-acetoxy and vic. chloro-tosylamino alcanes are the main products of the electrophilic reaction of chloramine T on olefins in acetic acid. The stereochemistry of the acetoxy chloration of the 2-butenes and cyclohexene is trans.

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