879207-98-4 Usage
Description
N-Boc-L-felinine, also known as N-(tert-butoxycarbonyl)-L-phenylalanine, is a synthetic amino acid derivative that plays a crucial role in the synthesis of various organic compounds and pharmaceuticals. It is characterized by the presence of a bulky tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom of the L-phenylalanine molecule, which provides stability during chemical reactions and facilitates selective deprotection when needed.
Uses
Used in Pharmaceutical Industry:
N-Boc-L-felinine is used as an intermediate in the synthesis of Felinine, a naturally occurring compound with potential therapeutic properties. Its role in the synthesis process is essential for the development of new drugs and pharmaceutical agents that can address various health conditions.
Used in Organic Synthesis:
N-Boc-L-felinine is also used as a versatile building block in organic synthesis, particularly for the preparation of complex organic molecules and bioactive compounds. The Boc protecting group allows for selective reactions to occur at specific functional groups, enabling the synthesis of a wide range of target molecules with high precision and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 879207-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,2,0 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 879207-98:
(8*8)+(7*7)+(6*9)+(5*2)+(4*0)+(3*7)+(2*9)+(1*8)=224
224 % 10 = 4
So 879207-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H25NO5S/c1-12(2,3)19-11(18)14-9(10(16)17)8-20-13(4,5)6-7-15/h9,15H,6-8H2,1-5H3,(H,14,18)(H,16,17)/t9-/m0/s1
879207-98-4Relevant articles and documents
Volatile organic sulfur-containing constituents in Poncirus trifoliata (L) Raf. (Rutaceae)
Starkenmann, Christian,Niclass, Yvan,Escher, Sina
, p. 4511 - 4517 (2008/09/20)
During our screening of plant materials to find new natural fragrance and flavor ingredients, we discovered two series of 3-sulfanylalkyl alkanoates in a peel extract of fruits of wild-growing Poncirus trifoliata (L) Raf. (Rutaceae), a species closely related to Citrus. The two series belong to alkanoates of 3-methyl-3-sulfanylbutan-1-ol and 3-sulfanylhexan-1-ol, respectively, and thus are members of a family of natural molecules having in common a 1,3-positioned O,S moiety. The alkanoate residues comprise all even-numbered saturated fatty acids from C2 (acetate) to C18 (octadecanoate). Among the 20 sulfur-containing compounds identified, 14 are described for the first time as naturally occurring in a botanical species. Several cysteine-S-conjugates were synthesized as hypothetical precursors of the new volatile sulfur-containing constituents, where after S-(3-hydroxy-1,1-dimethylpropyl)-L-cysteine, S-[3-(acetyloxy)-1,1- dimethylpropyl]-L-cysteine, and S-[1-(2-hydroxyethyl)butyl]-L-cysteine were identified in the fruit peel. No cysteine-S-conjugates were detected in the fruit juice.
