869882-71-3 Usage
Description
(S)-tert-Butyl 2-(((benzyloxy)carbonyl)-amino)-3-(4-nitrophenyl)propanoate is a complex chemical compound that is a derivative of propanoate. It features a tert-butyl group attached to a 2-(((benzyloxy)carbonyl)-amino)-3-(4-nitrophenyl) substituent, which gives it unique properties and potential applications in various fields.
Uses
Used in Organic Synthesis:
(S)-tert-Butyl 2-(((benzyloxy)carbonyl)-amino)-3-(4-nitrophenyl)propanoate is used as a reagent or intermediate in organic synthesis reactions. Its complex structure allows for the creation of a variety of compounds through chemical reactions.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (S)-tert-Butyl 2-(((benzyloxy)carbonyl)-amino)-3-(4-nitrophenyl)propanoate is used for the production of biologically active molecules. The presence of benzyloxy and nitrophenyl groups makes it a valuable component in the synthesis of pharmaceuticals.
Used in Medicinal Chemistry:
(S)-tert-Butyl 2-(((benzyloxy)carbonyl)-amino)-3-(4-nitrophenyl)propanoate is utilized in medicinal chemistry for its ability to modify the structure and properties of target molecules. This capability is crucial for the development of new drugs and therapeutic agents.
Used in Drug Discovery:
In the field of drug discovery, (S)-tert-Butyl 2-(((benzyloxy)carbonyl)-amino)-3-(4-nitrophenyl)propanoate plays a role in the identification and development of new drug candidates. Its unique structure and reactivity make it a promising compound for exploring novel therapeutic approaches.
Check Digit Verification of cas no
The CAS Registry Mumber 869882-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,8,8 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 869882-71:
(8*8)+(7*6)+(6*9)+(5*8)+(4*8)+(3*2)+(2*7)+(1*1)=253
253 % 10 = 3
So 869882-71-3 is a valid CAS Registry Number.
869882-71-3Relevant articles and documents
PREPARATION OF POLYMER CONJUGATES OF THERAPEUTIC, AGRICULTURAL, AND FOOD ADDITIVE COMPOUNDS
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Page/Page column 77-78, (2010/11/25)
Disclosed is a process for preparing polymer conjugates of agricultural, therapeutic, and food additive compounds using Mitsunobu conditions.
IMIDAZOLONE PHENYLALANINE DERIVATIVES AS VLA-4 ANTAGONISTS
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Page/Page column 59; 69-71, (2010/11/25)
Disclosed are compounds of the f ormula : and the pharmaceutically acceptable salts thereof wherein the variables A, n, R5, R21-R24 and Q are defined herein. These compounds bind VLA-4. Certain of these compound also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such compounds are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheimer's disease, atherosclerosis, AIDS dementia, diabetes, inflammatory bowel disease, rheumatoid arthritis, tissue transplantation, tumor metastasis and myocardial ischemia. The compounds can also be administered for the treatment of inflammatory brain diseases such as multiple sclerosis.