1037088-68-8 Usage
Description
(S)-methyl 2-amino-2-(3-nitrophenyl)acetate, with the molecular formula C9H10N2O4, is an amino acid derivative featuring a nitrophenyl group attached to the carbon atom. (S)-methyl 2-amino-2-(3-nitrophenyl)acetate possesses a chiral center, and the (S)-enantiomer is recognized as the active form. It is widely utilized in organic synthesis and pharmaceutical research, serving as a fundamental building block for the development of diverse compounds. The distinctive structure and properties of (S)-methyl 2-amino-2-(3-nitrophenyl)acetate render it a valuable asset in the creation of novel drugs and bioactive molecules, with potential applications in medicinal chemistry and drug discovery.
Uses
Used in Pharmaceutical Research:
(S)-methyl 2-amino-2-(3-nitrophenyl)acetate is used as a building block in pharmaceutical research for the development of new drugs and bioactive molecules. Its unique structure and properties allow for the creation of a variety of compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-methyl 2-amino-2-(3-nitrophenyl)acetate is used as a key intermediate for the synthesis of complex organic compounds. Its versatility and reactivity make it a valuable component in the construction of intricate molecular structures.
Used in Medicinal Chemistry:
(S)-methyl 2-amino-2-(3-nitrophenyl)acetate is employed as a crucial component in medicinal chemistry, where it aids in the design and synthesis of novel drug candidates. Its unique properties contribute to the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Drug Discovery:
In the realm of drug discovery, (S)-methyl 2-amino-2-(3-nitrophenyl)acetate is utilized as a starting material for the identification and optimization of potential drug candidates. Its distinctive structure and properties facilitate the exploration of new chemical space and the discovery of novel bioactive molecules with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 1037088-68-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,0,8 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1037088-68:
(9*1)+(8*0)+(7*3)+(6*7)+(5*0)+(4*8)+(3*8)+(2*6)+(1*8)=148
148 % 10 = 8
So 1037088-68-8 is a valid CAS Registry Number.
1037088-68-8Relevant articles and documents
ARYL-PHENYL-SULFONAMIDE-PHENYLENE COMPOUNDS AND THEIR USE
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Page/Page column 99, (2010/04/25)
The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain aryl-phenyl-sulfonamido-phenylene compounds of the following formula (I) (collectively referred to herein as "APSAP compounds"). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, in treatment, for example, of inflammation and/or joint destruction and/or bone loss; of disorders mediated by excessive and/or inappropriate and/or prolonged activation of the immune system; of inflammatory and autoimmune disorders, for example, rheumatoid arthritis, psoriasis, psoriatic arthritis, chronic obstructive pulmonary disease (COPD), atherosclerosis, inflammatory bowel disease, ankylosing spondylitis, and the like; of disorders associated with bone loss, such as bone loss associated with excessive osteoclast activity in rheumatoid arthritis, osteoporosis, cancer-associated bone disease, Paget's disease and the like, etc.; and of cancer, such as a haematological malignancy, a solid tumour, etc.
