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(tert-butoxycarbonyloxy)-2,4,6-trichlorobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53639-38-6

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53639-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53639-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,3 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53639-38:
(7*5)+(6*3)+(5*6)+(4*3)+(3*9)+(2*3)+(1*8)=136
136 % 10 = 6
So 53639-38-6 is a valid CAS Registry Number.

53639-38-6Downstream Products

53639-38-6Relevant academic research and scientific papers

A new, efficient, and catalyst-free microwave-assisted approach for formation of O-tert-butoxy carbonates

K'tir, Hacene,Amira, Aicha,Berredjem, Malika,Aouf, Nour-Eddine

supporting information, p. 851 - 853 (2014/06/23)

A new simple, efficient, greener, and catalyst-free chemoselective protocol for the O-tert-butoxycarbonylation of various structurally diverse hydroxy compounds was carried out with (Boc)2O under microwave radiation. The corresponding O-tertbutoxy carbonates were obtained in good to excellent yields in a short reaction time without any side reactions.

Organocatalytic methods for chemoselective O-tert-butoxycarbonylation of phenols and their regeneration from the O-t-Boc derivatives

Chankeshwara, Sunay V.,Chebolu, Rajesh,Chakraborti, Asit K.

supporting information; scheme or table, p. 8615 - 8618 (2009/04/11)

(Chemical Equation Presented) Carbon tetrabromide (CBr4) catalyzes O-tert-butoxycarbonylation of functionalized phenols without any side reactions (bromination, addition of CBr3 to a double bond, and formation of symmetrical diaryl carbonates, cyclic carbonates, or carbonic-carbonic anhydrides). The parent phenols are regenerated from the O-t-Boc derivatives by the catalyst system CBr4-PPh3 without affecting other protecting groups (aryl alkyl ether, alkyl ester, and thioacetal) or competitive side reaction such as bromination, nitrene (from NO2) and α,α-dibromoolefine (with CHO/COMe) formation, and transesterification (with CO2Me/Et) taking place.

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