167298-42-2 Usage
Description
[(1S)-1-(AMINOMETHYL)-2-PHENYLETHYL]-CARBAMIC ACID PHENYLMETHYL ESTER is an ester derivative of carbamic acid, characterized by the presence of an aminomethyl group and a phenylmethyl group attached to the carbamic acid through ester linkages. This white solid is soluble in organic solvents and is widely utilized in chemical synthesis and research as a reagent and intermediate for the production of pharmaceuticals and other organic compounds. Its structural features and reactivity also suggest potential applications in drug development and medicinal chemistry.
Uses
Used in Pharmaceutical Synthesis:
[(1S)-1-(AMINOMETHYL)-2-PHENYLETHYL]-CARBAMIC ACID PHENYLMETHYL ESTER is used as a reagent and intermediate in the pharmaceutical industry for the synthesis of various pharmaceuticals. Its unique structural features and reactivity make it a valuable component in the development of new drugs and therapeutic agents.
Used in Chemical Research:
In the field of chemical research, [(1S)-1-(AMINOMETHYL)-2-PHENYLETHYL]-CARBAMIC ACID PHENYLMETHYL ESTER serves as a crucial reagent for conducting experiments and exploring new chemical reactions. Its versatility in forming ester linkages with other compounds allows researchers to investigate a wide range of chemical properties and potential applications.
Used in Drug Development:
Due to its structural features and reactivity, [(1S)-1-(AMINOMETHYL)-2-PHENYLETHYL]-CARBAMIC ACID PHENYLMETHYL ESTER may have potential applications in drug development. It can be used as a building block for designing new molecules with specific biological activities, contributing to the advancement of novel therapeutic agents.
Used in Medicinal Chemistry:
In medicinal chemistry, [(1S)-1-(AMINOMETHYL)-2-PHENYLETHYL]-CARBAMIC ACID PHENYLMETHYL ESTER is employed as a key intermediate for the synthesis of complex organic compounds with potential medicinal properties. Its ability to form ester linkages and its compatibility with various organic solvents make it a valuable tool for creating new chemical entities with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 167298-42-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,2,9 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 167298-42:
(8*1)+(7*6)+(6*7)+(5*2)+(4*9)+(3*8)+(2*4)+(1*2)=172
172 % 10 = 2
So 167298-42-2 is a valid CAS Registry Number.
167298-42-2Relevant articles and documents
Serum stability of selected decapeptide agonists of KISS1R using pseudopeptides
Asami, Taiji,Nishizawa, Naoki,Ishibashi, Yoshihiro,Nishibori, Kimiko,Nakayama, Masaharu,Horikoshi, Yasuko,Matsumoto, Shin-Ichi,Yamaguchi, Masashi,Matsumoto, Hirokazu,Tarui, Naoki,Ohtaki, Tetsuya,Kitada, Chieko
, p. 6391 - 6396 (2012/11/07)
Metastin/kisspeptin, a 54-amino acid peptide, is the ligand of the G-protein-coupled receptor KISS1R which plays a key role in pathways that regulate reproduction and cell migration in many endocrine and gonadal tissues. The N-terminally truncated decapep
N-urethane-protected amino alkyl isothiocyanates: Synthesis, isolation, characterization, and application to the synthesis of thioureidopeptides
Sureshbabu, Vommina V.,Naik, Shankar A.,Hemantha,Narendra,Das, Ushati,Guru Row, Tayur N.
supporting information; experimental part, p. 5260 - 5266 (2009/12/06)
(Chemical Equation Presented) Synthetically useful N-Fmoc amino-alkyl isothiocyanates have been described, starting from protected amino acids. These compounds have been synthesized in excellent yields by thiocarbonylation of the monoprotected 1,2-diamines with CS2/TEA/p-TsCl, isolated as stable solids, and completely characterized. The procedure has been extended to the synthesis of amino alkyl isothiocyanates from Boc- and Z-protected amino acids as well. The utility of these isothiocyanates for peptidomimetics synthesis has been demonstrated by employing them in the preparation of a series of dithioureidopeptide esters. Boc-Gly-OH and Boc-Phe-OH derived isothiocyanates 9a and 9c have been obtained as single crystals and their structures solved through X-ray diffraction. They belong to the orthorhombic crystal system, and have a single molecule in the asymmetric unit (Z′ = 1). 9a crystallizes in the centrosymmetric space group Pbca, while 9c crystallizes in the noncentrosymmetric space group P212121.
A novel, simple, chemoseleetive and practical protocol for the reduction of azides using In/NH4Cl
Reddy, G. Vidyasagar,Rao, G. Venkat,Iyengar
, p. 3937 - 3938 (2007/10/03)
A simple, mild and efficient method for the reduction of azides to amines using In/NH4Cl is described.
