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(2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine is a chiral pyrrolidine derivative with a molecular formula of C28H29N3O4. It features a pyrrolidine ring to which a tert-butylphenyl group is attached at the 1-position and two 4-nitrophenyl groups are attached at the 2and 5-positions. (2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine is characterized by its highly symmetrical structure and the presence of two stereocenters at the 2and 5-positions, making it a valuable intermediate in organic synthesis and medicinal chemistry.

1258232-92-6

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1258232-92-6 Usage

Uses

Used in Organic Synthesis:
(2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structural features, including the presence of a pyrrolidine ring and multiple aromatic groups, make it a versatile component in the synthesis of a wide range of organic compounds.
Used in Medicinal Chemistry:
In the pharmaceutical industry, (2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine is utilized as a key intermediate in the development of various pharmaceuticals. Its chiral nature and structural diversity allow for the design and synthesis of enantiomerically pure drug candidates, which can exhibit improved pharmacological properties and reduced side effects.
Used in the Preparation of Bioactive Compounds:
(2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine is employed as an intermediate for the synthesis of diverse bioactive compounds. Its unique structural features enable the development of molecules with potential therapeutic applications, such as antimicrobial, antiviral, and anticancer agents.
Used in the Synthesis of Functional Materials:
(2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine is also used in the preparation of functional materials with specific properties, such as chiral catalysts, sensors, and chiral stationary phases for chromatographic separations. Its structural characteristics make it a valuable component in the design and synthesis of materials with tailored properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1258232-92-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,2,3 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1258232-92:
(9*1)+(8*2)+(7*5)+(6*8)+(5*2)+(4*3)+(3*2)+(2*9)+(1*2)=156
156 % 10 = 6
So 1258232-92-6 is a valid CAS Registry Number.

1258232-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,5S)-1-(4-tert-butylphenyl)-2,5-bis(4-nitrophenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names (2S,5S)-1-(4-(tert-butyl)phenyl)-2,5-bis(4-nitrophenyl)pyrrolidine

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:1258232-92-6 SDS

1258232-92-6Relevant academic research and scientific papers

ANTI-VIRAL COMPOUND

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Paragraph 0027, (2015/11/27)

The present invention features crystalline forms of Compound I.

Anti-Viral Compounds

-

, (2010/12/29)

Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.

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