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138624-05-2

Benzene, [4-(1-methylethylidene)cyclohexyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138624-05-2 Structure

  • Basic information

    1. Product Name: Benzene, [4-(1-methylethylidene)cyclohexyl]-
    2. Synonyms:
    3. CAS NO:138624-05-2
    4. Molecular Formula: C15H20
    5. Molecular Weight: 200.324
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138624-05-2.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: Benzene, [4-(1-methylethylidene)cyclohexyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzene, [4-(1-methylethylidene)cyclohexyl]-(138624-05-2)
    11. EPA Substance Registry System: Benzene, [4-(1-methylethylidene)cyclohexyl]-(138624-05-2)

  • 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: 138624-05-2(Hazardous Substances Data)

138624-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138624-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,2 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138624-05:
(8*1)+(7*3)+(6*8)+(5*6)+(4*2)+(3*4)+(2*0)+(1*5)=132
132 % 10 = 2
So 138624-05-2 is a valid CAS Registry Number.

138624-05-2Downstream Products

138624-05-2Relevant articles and documents

A mild radical procedure for the reduction of B-alkylcatecholboranes to alkanes

Pozzi, Davide,Scanlan, Eoin M.,Renaud, Philippe

, p. 14204 - 14205 (2007/10/03)

A mild radical-mediated reduction of organoboranes is reported. The reducing agent is methanol complexed by the Lewis acidic B-methoxycatecholborane. Copyright

Regioselective radical cyclization initiated by the reaction of allylic hydroperoxides with iron(II) sulfate

Masuyama, Araki,Sugawara, Tomohiro,Nojima, Masatomo,McCullough, Kevin J.

, p. 353 - 366 (2007/10/03)

Treatment of 1-methyl-2-methylene-1-cyclohexyl hydroperoxide with a mixture of FeSO4/CuCl2 yielded 1-(1-chlorocyclohexyl)ethanone as the major product consistent with 6-endo-trig cyclization of the intermediate 5-acetylhex-5-enyl rad

Triphenylbismuth dibromide-iodine: An efficient reagent for the dehydration of alcohols

Dorta,Dorta, Rosa L.,Suarez,Suarez, Ernesto,Betancor,Betancor, Carmen

, p. 5035 - 5038 (2007/10/02)

Tertiary and secondary alcohols react under mild conditions with triphenylbismuth dibromide and iodine under an inert atmosphere to give the corresponding most stable alkenes in good yields.

BF3·OEt2 promotes fast, mild, clean and regioselective dehydration of tertiary alcohols

Posner,Shulman-Roskes,Oh,Carry,Green,Clark,Dai,Anjeh

, p. 6489 - 6492 (2007/10/02)

BF3·OEt2 in methylene chloride at 25°C for 2 hours or less is shown to be effective for easy conversion of tertiary alcohols into the corresponding thermodynamically most stable alkenes.

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