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2-Isopropenyl-3,3-dimethyl-pent-4-enoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133036-70-1 Structure
  • Basic information

    1. Product Name: 2-Isopropenyl-3,3-dimethyl-pent-4-enoic acid ethyl ester
    2. Synonyms: 2-Isopropenyl-3,3-dimethyl-pent-4-enoic acid ethyl ester
    3. CAS NO:133036-70-1
    4. Molecular Formula:
    5. Molecular Weight: 196.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133036-70-1.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-Isopropenyl-3,3-dimethyl-pent-4-enoic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Isopropenyl-3,3-dimethyl-pent-4-enoic acid ethyl ester(133036-70-1)
    11. EPA Substance Registry System: 2-Isopropenyl-3,3-dimethyl-pent-4-enoic acid ethyl ester(133036-70-1)
  • 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: 133036-70-1(Hazardous Substances Data)

133036-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133036-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,3 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 133036-70:
(8*1)+(7*3)+(6*3)+(5*0)+(4*3)+(3*6)+(2*7)+(1*0)=91
91 % 10 = 1
So 133036-70-1 is a valid CAS Registry Number.

133036-70-1Downstream Products

133036-70-1Relevant articles and documents

Approaches to selective isoprenologation via reactions of (η3-allyl)Fe(CO)4+ with allyl nucleophiles

Li, Zhong,Nicholas, Kenneth M.

, p. 105 - 112 (2007/10/02)

The reactions of substituted (η3-allyl)Fe(CO)4BF4 complexes 1 with various allyl-metals and dienolate derivatives have been investigated in search of a method for regio- and stereocontrolled allyl-allyl coupling.All three classes of allyl derivatives react with 1 in moderate to good yield with variable regioselectivity; the silyl derivatives 2 generally provide good regioselectivity for attack at the less substituted terminus of unsymmetrical derivatives of 1 but deprotonation of the 1,1-dimethylallyl complex 1e prevents efficient isoprenylation.Although deprotonation of 1e also dominates with the siloxydienes, the lithium dienolates couple efficiently with 1; however, reaction at the α position of the dienolate dominates.

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