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CAS

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406720-50-1

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

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  • 406720-50-1 Structure

  • Basic information

    1. Product Name: tert-butyl 2-isopropylphenylcarbamate
    2. Synonyms: tert-butyl 2-isopropylphenylcarbamate
    3. CAS NO:406720-50-1
    4. Molecular Formula: C14H21NO2
    5. Molecular Weight: 235.32204
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 406720-50-1.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-isopropylphenylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 2-isopropylphenylcarbamate(406720-50-1)
    11. EPA Substance Registry System: tert-butyl 2-isopropylphenylcarbamate(406720-50-1)

  • 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: 406720-50-1(Hazardous Substances Data)

406720-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 406720-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,7,2 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 406720-50:
(8*4)+(7*0)+(6*6)+(5*7)+(4*2)+(3*0)+(2*5)+(1*0)=121
121 % 10 = 1
So 406720-50-1 is a valid CAS Registry Number.

406720-50-1Downstream Products

406720-50-1Relevant articles and documents

Mild deprotection of the: N-tert -butyloxycarbonyl (N -Boc) group using oxalyl chloride

Awuah, Samuel G.,George, Nathaniel,Ofori, Samuel,Parkin, Sean

, p. 24017 - 24026 (2020/07/23)

We report a mild method for the selective deprotection of the N-Boc group from a structurally diverse set of compounds, encompassing aliphatic, aromatic, and heterocyclic substrates by using oxalyl chloride in methanol. The reactions take place under room temperature conditions for 1-4 h with yields up to 90percent. This mild procedure was applied to a hybrid, medicinally active compound FC1, which is a novel dual inhibitor of IDO1 and DNA Pol gamma. A broader mechanism involving the electrophilic character of oxalyl chloride is postulated for this deprotection strategy. This journal is

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

The scope and limitations of deuteration mediated by Crabtree's catalyst

Ellames, George J,Gibson, Jennifer S,Herbert, John M,McNeill, Alan H

, p. 9487 - 9497 (2007/10/03)

Exchange of protons for deuterons mediated by Crabtree's catalyst, 1, is directed efficiently by a functional group containing an sp2-hybridised nitrogen or oxygen atom; more electron-rich substrates are, in general, deuterated more efficiently. The electronic effects of substituents in the arene ring are critical only where the directing group is poor, in which case exchange is generally promoted by electron donating substituents, but the exchange is impeded by bulky meta-substituents.

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