144599-95-1 Usage
Description
BOC-TRP(BOC)-OH, also known as N-Boc-1-Boc-L-tryptophan, is a chemical compound that serves as an intermediate in pharmaceutical and chemical research. It is characterized by its two BOC (tert-butoxycarbonyl) protecting groups, which play a crucial role in protecting the tryptophan molecule during various chemical reactions.
Uses
BOC-TRP(BOC)-OH is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs and compounds. The expression is: BOC-TRP(BOC)-OH is used as a chemical intermediate for the synthesis of pharmaceutical compounds.
Used in Pharmaceutical Research:
BOC-TRP(BOC)-OH is used as a key building block in the development of new drugs and therapeutic agents. Its application in this field is due to its ability to be incorporated into complex molecular structures, which can then be further modified and optimized for specific medical applications.
Used in Chemical Research:
In the field of chemical research, BOC-TRP(BOC)-OH is utilized as a versatile starting material for the synthesis of a wide range of chemical compounds. Its use in this industry is attributed to the protective nature of the BOC groups, which allow for selective reactions and the formation of diverse chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 144599-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144599-95:
(8*1)+(7*4)+(6*4)+(5*5)+(4*9)+(3*9)+(2*9)+(1*5)=171
171 % 10 = 1
So 144599-95-1 is a valid CAS Registry Number.
144599-95-1Relevant articles and documents
Mild and selective deprotection of carbamates with Bu4NF
Jacquemard, Ulrich,Bénéteau, Valérie,Lefoix, Myriam,Routier, Sylvain,Mérour, Jean-Yves,Coudert, Gérard
, p. 10039 - 10047 (2007/10/03)
A new mild method allowing the removal of carbamates using TBAF in THF is reported. Reactions were performed on indole, indoline, N-methyl aniline, aniline and tryptamine derivatives. The observed selectivity according to the carbamates or the substrates is discussed. A mechanism is postulated. Graphical Abstract