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1-[4-deutero-2-(deuteromethyl)butyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133124-42-2 Structure
  • Basic information

    1. Product Name: 1-[4-deutero-2-(deuteromethyl)butyl]benzene
    2. Synonyms: 1-[4-deutero-2-(deuteromethyl)butyl]benzene
    3. CAS NO:133124-42-2
    4. Molecular Formula:
    5. Molecular Weight: 150.232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133124-42-2.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: 1-[4-deutero-2-(deuteromethyl)butyl]benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[4-deutero-2-(deuteromethyl)butyl]benzene(133124-42-2)
    11. EPA Substance Registry System: 1-[4-deutero-2-(deuteromethyl)butyl]benzene(133124-42-2)
  • 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: 133124-42-2(Hazardous Substances Data)

133124-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133124-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,1,2 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133124-42:
(8*1)+(7*3)+(6*3)+(5*1)+(4*2)+(3*4)+(2*4)+(1*2)=82
82 % 10 = 2
So 133124-42-2 is a valid CAS Registry Number.

133124-42-2Downstream Products

133124-42-2Relevant articles and documents

Zirconium-catalyzed reaction of terminal alkenes with triethylindium

Ramazanov,Dil'Mukhametova,Dzhemilev

, p. 1253 - 1256 (2013)

Terminal alkenes (undec-1-ene, oct-1-ene, and allylbenzene) reacted with triethylindium in the presence of a catalytic amount of Cp2ZrCl 2 in hexane to give mixtures of three organoindium compounds whose hydrolysis in D2O afforded 2-substituted 1,4-dideuterobutane containing minor amounts of 2-substituted 1- and 4-deuterobutanes.

Catalytic enantioselective ethylalumination of terminal alkenes: Substrate effects and absolute configuration assignment

Parfenova, Lyudmila V.,Kovyazin, Pavel V.,Tyumkina, Tatyana V.,Makrushina, Alyona V.,Khalilov, Leonard M.,Dzhemilev, Usein M.

, p. 124 - 135 (2015/02/19)

The chemo- and enantioselectivity of the reaction of alkenes with AlEt3 catalyzed by bis(1-neomenthylindenyl)zirconium dichloride has been studied. The reaction with linear alkenes in a chlorinated solvent (CH2Cl2) gives m

Cyclomagnesation of olefins with ethylmagnesium bromide in the presence of titanium complexes

Dzhemilev,D'yakonov,Khafizova,Ibragimov

, p. 352 - 357 (2007/10/03)

Cyclomagnesation of terminal and cyclic olefins and 1,2-dienes with RMgHlg and R2Mg in the presence of dichloro(dicyclopentadienyl)titanium(IV) gives non-Grignard cyclic and acyclic organomagnesium compounds. The reaction direction depends on t

SYNTHESIS AND TRANSFORMATIONS OF METALLOCYCLES. 5. REGIOSELECTIVE SYNTHESIS OF β-SUBSTITUTED ALUMOCYCLOPENTANES BY THE CYCLOMETALLATION OF α-OLEFINS USING Et3Al IN THE PRESENCE OF Cp2ZrCl2

Dzhemilev, U. M.,Ibragimov, A. G.,Zolotarev, A. P.,Muslukhov, R. R.,Tolstokov, G. A.

, p. 2570 - 2578 (2007/10/02)

A new method has been proposed for the synthesis of N-, O-, and S-containing alumocyclopentanes by the reaction of Et3Al with functional α-olefins in the presence of catalytic amounts of Cp2ZrCl2.The alumocyclopentanes obtained may react with S8 to give β-substituted tetrahydrothiophenes.

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