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119407-12-4

Carbamic acid, cyclohexyl[(trimethylsilyl)methyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119407-12-4 Structure

  • Basic information

    1. Product Name: Carbamic acid, cyclohexyl[(trimethylsilyl)methyl]-, methyl ester
    2. Synonyms:
    3. CAS NO:119407-12-4
    4. Molecular Formula: C12H25NO2Si
    5. Molecular Weight: 243.421
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119407-12-4.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: Carbamic acid, cyclohexyl[(trimethylsilyl)methyl]-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, cyclohexyl[(trimethylsilyl)methyl]-, methyl ester(119407-12-4)
    11. EPA Substance Registry System: Carbamic acid, cyclohexyl[(trimethylsilyl)methyl]-, methyl ester(119407-12-4)

  • 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: 119407-12-4(Hazardous Substances Data)

119407-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119407-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,0 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119407-12:
(8*1)+(7*1)+(6*9)+(5*4)+(4*0)+(3*7)+(2*1)+(1*2)=114
114 % 10 = 4
So 119407-12-4 is a valid CAS Registry Number.

119407-12-4Relevant articles and documents

Highly selective Friedel-Crafts monoalkylation using micromixing

Suga, Seiji,Nagaki, Aiichiro,Yoshida, Jun-Icih

, p. 354 - 355 (2003)

Highly selective Friedel-Crafts monoalkylation of aromatic compounds with N-acyliminium ions has been achieved by efficient 1:1 mixing using a multilamination-type micromixer.

Control of extremely fast competitive consecutive reactions using micromixing. Selective Friedel-Crafts aminoalkylation

Nagaki, Aiichiro,Togai, Manabu,Suga, Seiji,Aoki, Nobuaki,Mae, Kazuhiro,Yoshida, Jun-Ichi

, p. 11666 - 11675 (2005)

Friedel-Crafts reactions of aromatic and heteroaromatic compounds with an N-acyliminium ion pool were studied. The reaction of 1,3,5-trimethylbenzene in a batch reactor gave rise to the selective formation of a monoalkylation product (69%). Presumably, th

ELECTROCHEMICAL OXIDATION OF α-SILYLCARBAMATES

Yoshida, Jun-ichi,Isoe, Sachihiko

, p. 6621 - 6624 (2007/10/02)

α-Silyl group activates carbamates toward electrochemical oxidation which results in facile cleavage of carbon-silicon bond and regioselective introduction of methanol at α-carbon.

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