118329-81-0 Usage
Description
(2S,4R)-2-ethoxycarbonyl-1-(toluene-4-sulfonyl)-4-(toluene-4-sulfonyloxy)pyrrolidine is a heterocyclic organic compound derived from pyrrolidine. It features a pyrrolidine ring with ethoxycarbonyl, toluene-4-sulfonyl, and toluene-4-sulfonyloxy substituents attached to different positions of the ring. The ethoxycarbonyl group is a carbonyl group attached to an ethoxy group, while the toluene-4-sulfonyl groups are sulfonate ester groups attached to the pyrrolidine ring. This unique structure and reactivity may offer potential applications in various fields.
Uses
Used in Organic Synthesis:
(2S,4R)-2-ethoxycarbonyl-1-(toluene-4-sulfonyl)-4-(toluene-4-sulfonyloxy)pyrrolidine is used as a synthetic intermediate for the development of complex organic molecules. Its unique functional groups allow for versatile chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2S,4R)-2-ethoxycarbonyl-1-(toluene-4-sulfonyl)-4-(toluene-4-sulfonyloxy)pyrrolidine is used as a key component in the design and synthesis of novel drug candidates. Its specific stereochemistry and functional groups can be exploited to create molecules with desired biological activities, potentially leading to the development of new therapeutic agents.
Used in Chemical Research:
(2S,4R)-2-ethoxycarbonyl-1-(toluene-4-sulfonyl)-4-(toluene-4-sulfonyloxy)pyrrolidine serves as a valuable research tool in chemical research. Its unique structure and reactivity can be studied to gain insights into various chemical processes and mechanisms, contributing to the advancement of scientific knowledge in the field of organic chemistry.
Further studies and research may be necessary to fully understand the properties and potential uses of this compound, as its applications may extend beyond the current understanding.
Check Digit Verification of cas no
The CAS Registry Mumber 118329-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,2 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118329-81:
(8*1)+(7*1)+(6*8)+(5*3)+(4*2)+(3*9)+(2*8)+(1*1)=130
130 % 10 = 0
So 118329-81-0 is a valid CAS Registry Number.
118329-81-0Relevant articles and documents
The first asymmetric synthesis of (2S,3S,4R)-3-amino-2-hydroxymethyl-4- hydroxypyrrolidine
Curtis, Kim L.,Fawcett, John,Handa, Sandeep
, p. 5297 - 5300 (2005)
The novel (2S,3S,4R)-3-amino-2-hydroxymethyl-4-hydroxypyrrolidine 5 has been produced in an efficient synthesis from trans-4-hydroxy-l-proline 8. The key step involves a tethered aminohydroxylation of the alkene 7 to introduce regio- and stereoselectively
Benzyl compounds which inhibit leukocyte adhesion mediated by VLA-4
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Page column 63, (2010/01/31)
Disclosed are compounds which bind VLA-4. Certain of these compounds 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, wherein the disease may be, for example, 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.
