412279-18-6 Usage
Uses
Used in Pharmaceutical Research and Development:
2-Pyrrolidinecarboxamide,3-hydroxy-,(2S,3S)-(9CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Pyrrolidinecarboxamide,3-hydroxy-,(2S,3S)-(9CI) serves as a versatile starting material for the preparation of a wide range of organic compounds. Its reactivity and functional groups allow for various chemical transformations, enabling the synthesis of complex molecules with diverse applications.
Used in Medicinal Chemistry:
2-Pyrrolidinecarboxamide,3-hydroxy-,(2S,3S)-(9CI) is utilized in medicinal chemistry for the design and synthesis of novel bioactive molecules. Its unique structural features and functional groups can be exploited to create new compounds with potential therapeutic properties, contributing to the discovery of innovative treatments for various diseases and conditions.
Used in the Production of New Materials and Compounds:
In addition to its applications in pharmaceutical research and organic synthesis, 2-Pyrrolidinecarboxamide,3-hydroxy-,(2S,3S)-(9CI) also has potential uses in the development of new materials and compounds. Its unique properties can be harnessed to create novel substances with specific characteristics, opening up new avenues for research and innovation in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 412279-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,2,7 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 412279-18:
(8*4)+(7*1)+(6*2)+(5*2)+(4*7)+(3*9)+(2*1)+(1*8)=126
126 % 10 = 6
So 412279-18-6 is a valid CAS Registry Number.
412279-18-6Relevant articles and documents
Organic Compounds
-
Page/Page column 38, (2009/07/10)
The present invention relates to compounds of formula I and its salts, wherein the substituents are as defined in the description, to compositions and use of the compounds in the treatment of diseases ameloriated by inhibition of phosphatidylinositol 3-kinase.
ORGANIC COMPOUNDS
-
Page/Page column 43, (2009/07/25)
The resent invention relates to a com ound of formula (I) and its salts, wherein the substituents are as defined in the description, to compositions and use of the compounds in the treatment of diseases ameloriated by inhibition of phosphatidylinositol 3-
2-Substituted Penems with Amino Acid-Related Side Chains: Synthesis and Antibacterial Activity of a New Series of β-Lactam Antibiotics
Altamura, Maria,Perrotta, Enzo,Sbraci, Piero,Pestellini, Vittorio,Arcamone, Federico,et al.
, p. 4244 - 4256 (2007/10/03)
A new series of 6-(hydroxyethyl)penems 2-substituted with amino acid-related side chains was synthesized.The nature of the amino acyl derivative proved to be crucial both from a synthetic point of view, as β-lactam ring opening can compete with C-2 nucleophilic substitution, and for antibacterial activity.Primary amino acid amides emerged as the most suitable side chains for enhancing permeability through a Gram-negative outer membrane.In vitro activity of the new 2-penems 3a-u was influenced by the nature and position of the amide moiety, the ring size for cyclic amides, and the configuration of the amino acid.Compounds bearing amides derived from small N-methyl amino acids (such as 3a) or from cyclic amino acids (such as prolinamide 3p and 4-hydroxyprolinamide 3r) showed broad spectrum in vitro activity against both Gram-positive and Gram-negative microorganisms.
