98628-27-4 Usage
Description
Boc-L-2-Amino-5-phenyl-pentanoic acid is a peptide chemical compound with the molecular formula C18H25NO4. It features a protecting group named Boc (tert-butyloxycarbonyl) attached to the N-terminal of the amino acid L-2-Amino-5-phenyl-pentanoic acid. This unique structure and its properties make it an important reagent in organic and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
Boc-L-2-Amino-5-phenyl-pentanoic acid is used as a building block for the preparation of complex organic molecules and in the synthesis of peptides and pharmaceuticals. Its ability to protect amino acid residues during chemical reactions is crucial for the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, Boc-L-2-Amino-5-phenyl-pentanoic acid serves as an essential reagent for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 98628-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98628-27:
(7*9)+(6*8)+(5*6)+(4*2)+(3*8)+(2*2)+(1*7)=184
184 % 10 = 4
So 98628-27-4 is a valid CAS Registry Number.
98628-27-4Relevant articles and documents
Organocatalytic one-pot oxidative cleavage of terminal diols to dehomologated carboxylic acids
Shibuya, Masatoshi,Doi, Ryusuke,Shibuta, Takuro,Uesugi, Shun-Ichiro,Iwabuchi, Yoshiharu
, p. 5006 - 5009 (2013/01/15)
The organocatalytic one-pot oxidative cleavage of terminal 1,2-diols to one-carbon-unit-shorter carboxylic acids is described. The combination of 1-Me-AZADO (cat.), NaOCl (cat.), and NaClO2 caused smooth one-pot oxidative cleavage under mild conditions. A broad range of substrates including carbohydrates and N-protected amino diols were converted without epimerization. Terminal triols and tetraols respectively underwent cleavage of their C-2 and C-3 moieties to afford their corresponding two- and three-carbon-unit-shorter carboxylic acids.
Solid-phase synthesis of dehydropeptide, AM-toxin II, using a novel selenyl linker by side-chain tethered strategy
Horikawa, Eiji,Kodaka, Masato,Nakahara, Yoshiaki,Okuno, Hiroaki,Nakamura, Kazuhiko
, p. 8337 - 8339 (2007/10/03)
The cyclic dehydrodepsipeptide, AM-toxin II, was efficiently synthesized by a solid-phase method using a novel selenyl linker. The cleavage from the resin with formation of a double bond is successfully achieved under mild oxidative conditions with TBHP.