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54145-10-7

Carbamic acid, [[(4-methylphenyl)sulfonyl]oxy]-, 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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  • 54145-10-7 Structure

  • Basic information

    1. Product Name: Carbamic acid, [[(4-methylphenyl)sulfonyl]oxy]-, ethyl ester
    2. Synonyms:
    3. CAS NO:54145-10-7
    4. Molecular Formula: C10H13NO5S
    5. Molecular Weight: 259.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54145-10-7.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, [[(4-methylphenyl)sulfonyl]oxy]-, ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [[(4-methylphenyl)sulfonyl]oxy]-, ethyl ester(54145-10-7)
    11. EPA Substance Registry System: Carbamic acid, [[(4-methylphenyl)sulfonyl]oxy]-, ethyl ester(54145-10-7)

  • 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: 54145-10-7(Hazardous Substances Data)

54145-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54145-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,4 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54145-10:
(7*5)+(6*4)+(5*1)+(4*4)+(3*5)+(2*1)+(1*0)=97
97 % 10 = 7
So 54145-10-7 is a valid CAS Registry Number.

54145-10-7Relevant articles and documents

An Effective Method for the Synthesis of 1,3-Dihydro-2H-indazoles via N-N Bond Formation

Zhang, Xiaoke,Pan, Yang,Liang, Peng,Ma, Xiaofeng,Jiao, Wei,Shao, Huawu

supporting information, p. 5552 - 5557 (2019/11/22)

The [4+1] cycloaddition reaction of bifunctional amino reagents has been achieved with in situ formed aza-ortho-quinone methides. Specifically, N-(tosyloxy)carbamates were used as an N1 synthon and bifunctional amino reagents for this transformation, which provides a metal-free, catalyst-free, and oxidant-free strategy to form nitrogen-nitrogen bonds. (Figure presented.).

Osmium-catalyzed vicinal oxyamination of alkenes by N-(4- toluenesulfonyloxy)carbamates

Masruri,Willis, Anthony C.,McLeod, Malcolm D.

, p. 8480 - 8491 (2012/11/13)

N-(4-Toluenesulfonyloxy)carbamates based on a range of common amine protecting groups serve as preformed nitrogen sources in the intermolecular osmium-catalyzed oxyamination reaction of a variety of mono-, di-, and trisubstituted alkenes. The reactions occur with low catalyst loadings and good yields and afford high regioselectivity for unsymmetrically substituted alkenes.

Cs2CO3 or CaO as promoters of ethyl N-{[(4-methylphenyl)sulphonyl]oxy}carbamate in amination reactions

Barani, Marco,Fioravanti, Stefania,Pellacani, Lucio,Tardella, Paolo A.

, p. 11235 - 11238 (2007/10/02)

Replacing triethylamine by heterogeneous inorganic bases makes it possible to aminate benzene or other nitrene acceptors, using the title reagent, previously reported to be scarcely reactive. Products of C-H insertion and/or those coming from intermediate aziridines are also obtained.

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