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164083-60-7

tert-butyl 2,5-dimethylphenylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 164083-60-7 Structure

  • Basic information

    1. Product Name: tert-butyl 2,5-dimethylphenylcarbamate
    2. Synonyms: tert-butyl 2,5-dimethylphenylcarbamate
    3. CAS NO:164083-60-7
    4. Molecular Formula: C13H19NO2
    5. Molecular Weight: 221.29546
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164083-60-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-butyl 2,5-dimethylphenylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 2,5-dimethylphenylcarbamate(164083-60-7)
    11. EPA Substance Registry System: tert-butyl 2,5-dimethylphenylcarbamate(164083-60-7)

  • 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: 164083-60-7(Hazardous Substances Data)

164083-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164083-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,0,8 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 164083-60:
(8*1)+(7*6)+(6*4)+(5*0)+(4*8)+(3*3)+(2*6)+(1*0)=127
127 % 10 = 7
So 164083-60-7 is a valid CAS Registry Number.

164083-60-7Relevant articles and documents

Organocatalytic Para-Selective Amination of Phenols with Iminoquinone Monoacetals

Liu, Liu,Chen, Kun,Wu, Wen-Zhen,Wang, Peng-Fei,Song, Hang-Yu,Sun, Hongbin,Wen, Xiaoan,Xu, Qing-Long

supporting information, p. 3823 - 3826 (2017/07/26)

A highly selective para C-H amination of unprotected phenols with iminoquinone acetals was realized, giving the functional phenols in good to excellent yields. Overall, this transformation is operationally simple, proceeds with readily available phenols, and has wide substrate scope and low catalyst loading. The biarylamine product is stochastically formed via [5,5]-sigmatropic rearrangement of a mixed acetal species which is generated in situ under the reaction conditions.

Cyclization-carbonylation-cyclization coupling reactions of N-propargylanilines and o-alkynylphenols with palladium(II)-bisoxazoline catalysts

Kusakabe, Taichi,Sekiyama, Emika,Ishino, Yukari,Motodate, Satoshi,Kato, Shigeki,Mochida, Tomoyuki,Kato, Keisuke

supporting information; experimental part, p. 1825 - 1832 (2012/07/30)

Cyclization-carbonylation-cyclization coupling reactions (CCC-coupling reactions) of N-propargylanilines and o-alkynylphenols catalyzed by (box)Pd(II) complexes afforded symmetrical bis(quinolin-3-yl) and bis(benzofuran-3-yl) ketones, respectively, in mod

Room-temperature Pd-catalyzed amidation of aryl bromides using tert-butyl carbamate

Bhagwanth, Swapna,Waterson, Alex G.,Adjabeng, George M.,Hornberger, Keith R.

supporting information; experimental part, p. 4634 - 4637 (2009/09/08)

(Chemical Equation Presented) The scope of Pd-catalyzed synthesis of N-Boc-protected anilines from aryl bromides and commercially available tertbutyl carbamate is described. For the first time, this process can be conducted at room temperature (17-22°C) u

1H-INDOLE-3-ACETAMIDE SPLA2 INHIBITORS

-

, (2008/06/13)

A class of novel 1-indole-3-acetamides represented by the formula; is disclosed together with the use of such indole compounds for inhibiting sPLA2 mediated release of fatty acids.

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