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CAS

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81617-12-1

1-(2-methyl-3-butenyloxy)-4-(1,1-dimethylethyl)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81617-12-1 Structure

  • Basic information

    1. Product Name: 1-(2-methyl-3-butenyloxy)-4-(1,1-dimethylethyl)cyclohexane
    2. Synonyms: 1-(2-methyl-3-butenyloxy)-4-(1,1-dimethylethyl)cyclohexane
    3. CAS NO:81617-12-1
    4. Molecular Formula:
    5. Molecular Weight: 224.387
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81617-12-1.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: 1-(2-methyl-3-butenyloxy)-4-(1,1-dimethylethyl)cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-methyl-3-butenyloxy)-4-(1,1-dimethylethyl)cyclohexane(81617-12-1)
    11. EPA Substance Registry System: 1-(2-methyl-3-butenyloxy)-4-(1,1-dimethylethyl)cyclohexane(81617-12-1)

  • 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: 81617-12-1(Hazardous Substances Data)

81617-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81617-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,1 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81617-12:
(7*8)+(6*1)+(5*6)+(4*1)+(3*7)+(2*1)+(1*2)=121
121 % 10 = 1
So 81617-12-1 is a valid CAS Registry Number.

81617-12-1Downstream Products

81617-12-1Relevant articles and documents

Reaction of 2-Methoxyethyl Hemiacetals with Allylsilanes in the Presence of Titanium Tetrachloride: Regioselective C-O Bond Cleavage of the Unsymmetrical Acetals

Nishiyama, Hisao,Itoh, Kenji

, p. 2496 - 2498 (2007/10/02)

Reaction of 2-methoxyethyl hemiacetals with allylsilanes in the presence of titanium tetrachloride gave the corresponding homoallyl ethers in good yields by the regioselective C-O bond cleavage of the hemiacetals.A new carbon homologative cyclization was

Reaction of Allylsilanes and Monothioacetals in the Presence of Lewis Acids: Regioselectivity in the Cleavage of the Acetals

Nishiyama, Hisao,Narimatsu, Shinzo,Sakuta, Koji,Itoh, Kenji

, p. 459 - 460 (2007/10/02)

Trimethylallylsilane reacts with monothioacetals in the presence of tin(IV) chloride, titanium tetrachloride, or boron trifluoride-diethyl ether to give the homoallyl ethers and homoallyl sulphides.

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