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Tert-butyl 4-(2-oxo-4-phenyl-2,3-dihydroimidazol-1-yl)piperidine-1-carboxylate is a complex heterocyclic chemical compound belonging to the class of piperidine derivatives. It features a carbamate ester with a tert-butyl group attached to the piperidine ring, along with a phenyl group and an imidazole ring, which contribute to its unique structure and potential pharmacological properties. tert-butyl 4-(2-oxo-4-phenyl-2,3-dihydroimidazol-1-yl)piperidine-1-carboxylate is often utilized in organic synthesis and pharmaceutical research due to its distinctive characteristics and the possibility of its use in the development of new drugs or as a building block for synthesizing other biologically active compounds.

205058-11-3

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205058-11-3 Usage

Uses

Used in Pharmaceutical Research:
Tert-butyl 4-(2-oxo-4-phenyl-2,3-dihydroimidazol-1-yl)piperidine-1-carboxylate is used as a research compound for its potential pharmacological properties, which may contribute to the development of new drugs. Its unique structure allows it to be a promising candidate for various therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, tert-butyl 4-(2-oxo-4-phenyl-2,3-dihydroimidazol-1-yl)piperidine-1-carboxylate is used as a building block for the synthesis of other compounds with biological activity. Its complex heterocyclic nature makes it a valuable component in creating novel molecules with potential applications in medicine and other industries.
Used in Drug Development:
Tert-butyl 4-(2-oxo-4-phenyl-2,3-dihydroimidazol-1-yl)piperidine-1-carboxylate is used as a precursor in drug development, where its unique structure can be leveraged to create new pharmaceutical agents. Its presence in a compound may enhance the pharmacological profile, leading to improved therapeutic effects.
Used in Chemical Industry:
In the chemical industry, tert-butyl 4-(2-oxo-4-phenyl-2,3-dihydroimidazol-1-yl)piperidine-1-carboxylate may be used as an intermediate in the synthesis of various chemical products, taking advantage of its reactivity and structural features to produce a range of valuable end products.

Check Digit Verification of cas no

The CAS Registry Mumber 205058-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,0,5 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 205058-11:
(8*2)+(7*0)+(6*5)+(5*0)+(4*5)+(3*8)+(2*1)+(1*1)=93
93 % 10 = 3
So 205058-11-3 is a valid CAS Registry Number.

205058-11-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(2-oxo-5-phenyl-1H-imidazol-3-yl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-Butyl 4-(2-oxo-4-phenyl-2,3-dihydro-1H-imidazol-1-yl)piperidine-1-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:205058-11-3 SDS

205058-11-3Relevant academic research and scientific papers

NOVEL HETEROCYCLIC COMPOUNDS AND USE THEREOF IN MEDICINE AND IN COSMETICS

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Paragraph 1388, (2018/03/25)

The invention relates to novel heterocyclic compounds of general formula (I), as well as their pharmaceutically acceptable salts, and their enantiomers. The invention also relates to the use thereof as a medicinal product, preferably in the prevention and/or treatment of inflammatory diseases with a neurogenic component or use thereof as a cosmetic. The compounds of the present invention act as antagonists of the CGRP-R receptor.

CGRP receptor antagonists

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Page/Page column 137, (2008/06/13)

The present invention relates to CGRP receptor antagonists, pharmaceutical compositions thereof, and methods therewith for treating CGRP receptor-mediated diseases and conditions.

Development of human calcitonin gene-related peptide (CGRP) receptor antagonists. 1. Potent and selective small molecule CGRP antagonists. 1-[N 2-[3,5-dibromo-N-[[4-(3,4-dihydro-2(1H)-oxoquinazolin-3-yl) -1-piperidinyl]carbonyl]-D-tyrosyl]-L-ly

Rudolf, Klaus,Eberlein, Wolfgang,Engel, Wolfhard,Pieper, Helmut,Entzeroth, Michael,Hallermayer, Gerhard,Doods, Henri

, p. 5921 - 5931 (2007/10/03)

Although the triptans have greatly improved the acute treatment of migraine headache, there are yet many shortcomings. Therefore, new strategies for the treatment of migraine are needed which offer advantages over current therapy, e.g. triptans. Our novel

Modified aminoacids, pharmaceuticals containing these compounds and method for their production

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Example A1a), (2008/06/13)

The present invention relates to modified amino acids of general formula wherein A, Z, X, n, m, R, R2, R3, R4and R11are defined as in claims 1 to 5, their tautomers, their diastereomers, their enantiomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, pharmaceutical compositions containing these compounds, the use thereof and processes for preparing them as well as their use for the production and purification of antibodies and as labelled compounds in RIA- and ELISA assays and as diagnostic or analytical aids in neurotransmitter research.

Modified amino acids, pharmaceuticals containing these compounds and method for their production

-

, (2008/06/13)

The present invention relates to modified amino acids of general formula wherein A, Z, X, n, m, R, R2, R3, R4 and R11 are defined as in claims 1 to 5, their tautomers, their diastereomers, their enantiomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, pharmaceutical compositions containing these compounds, the use thereof and processes for preparing them as well as their use for the production and purification of antibodies and as labelled compounds in RIA- and ELISA assays and as diagnostic or analytical aids in neurotransmitter research.

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