3060-50-2 Usage
Description
2,2-Diphenylglycine is a highly similar analogue and the simplest aromatic peptide, characterized by its white powder chemical properties. It can be utilized as a synthesis reagent for amination reactions and serves as a useful intermediate in pharmaceutical and organic synthesis. Additionally, its derivatives have demonstrated anticonvulsant activity, making them potential candidates for the treatment of pain.
Uses
Used in Pharmaceutical Industry:
2,2-Diphenylglycine is used as a synthesis reagent for amination reactions, playing a crucial role in the development of various pharmaceutical products. Its ability to act as an intermediate in organic synthesis contributes to the creation of a wide range of medications.
Used in Organic Synthesis:
In the field of organic synthesis, 2,2-Diphenylglycine is employed as an intermediate, enabling the production of a diverse array of organic compounds. Its unique properties and reactivity make it a valuable component in the synthesis of various molecules.
Used in Anticonvulsant Applications:
The derivatives of 2,2-Diphenylglycine have shown anticonvulsant activity, making them useful in the treatment of pain and potentially other related conditions. This application highlights the compound's versatility and its potential impact on healthcare.
References
And, Meital Reches, and E. Gazit. "Formation of Closed-Cage Nanostructures by Self-Assembly of Aromatic Dipeptides." Nano Letters 4.4(2006):581-585.
https://www.alfa.com/en/catalog/B22650/
Harris, Robert H. "New uses for amino acid anticonvulsants for treatment of pain." EP, WO/2002/015922. 2002.
Check Digit Verification of cas no
The CAS Registry Mumber 3060-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,6 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3060-50:
(6*3)+(5*0)+(4*6)+(3*0)+(2*5)+(1*0)=52
52 % 10 = 2
So 3060-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO2/c15-14(13(16)17,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,15H2,(H,16,17)
3060-50-2Relevant articles and documents
Versatile synthesis of free and N-benzyloxycarbonyl-protected 2,2-disubstituted taurines
Wang, Boyuan,Zhang, Wei,Zhang, Leilei,Du, Da-Ming,Liu, Gang,Xu, Jiaxi
, p. 350 - 355 (2008/09/18)
An effective and versatile method was developed to synthesize N-benzyloxycarbonyl-protected and free 2,2-disubstituted taurines. Several novel 2,2-disubstituted taurines, including aliphatic/aromatic and cyclic/acyclic derivatives, were obtained, which demonstrates the generality of this method. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
PHENYLATION OF AMINO ACID DERIVATIVES: A NEW ROUTE TO Α-PHENYL-Α-SUBSTITUTED AMINO ACIDS
O'Donnell, Martin J.,Bennett, William D.,Jacobsen, William N.,Ma, You-an
, p. 3913 - 3914 (2007/10/02)
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UNUSUAL CASE OF THE APPEL REACTION
Zhmurova, I. N.,Yurchenko, V. G.
, p. 42 - 45 (2007/10/02)
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