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(1S,4S)-4-(2,5-diMethyl-1H-pyrrol-1-yl)-1-(propan-2-yl)cyclopent-2-ene-1-carboxylic acid is a complex organic compound belonging to the carboxylic acid class. It features a cyclopentene ring with a substituted pyrrole group and exhibits chirality, indicated by its (1S,4S) stereochemistry. The unique molecular structure and properties of (1S,4S)-4-(2,5-diMethyl-1H-pyrrol-1-yl)-1-(propan-2-yl)cyclopent-2-ene-1-carboxylic acid make it a promising candidate for various pharmaceutical, chemical, and biological applications, warranting further research and development for specific uses.

851916-39-7

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851916-39-7 Usage

Uses

Used in Pharmaceutical Industry:
(1S,4S)-4-(2,5-diMethyl-1H-pyrrol-1-yl)-1-(propan-2-yl)cyclopent-2-ene-1-carboxylic acid is used as a pharmaceutical compound for its potential therapeutic effects. Its unique structure and chirality may contribute to the development of new drugs with specific targeting and activity profiles.
Used in Chemical Industry:
In the chemical industry, (1S,4S)-4-(2,5-diMethyl-1H-pyrrol-1-yl)-1-(propan-2-yl)cyclopent-2-ene-1-carboxylic acid can be utilized as a building block or intermediate in the synthesis of other complex organic molecules. Its unique functional groups and stereochemistry may enable the creation of novel chemical entities with specialized applications.
Used in Biological Research:
(1S,4S)-4-(2,5-diMethyl-1H-pyrrol-1-yl)-1-(propan-2-yl)cyclopent-2-ene-1-carboxylic acid is employed in biological research as a tool compound. Its unique properties may allow for the investigation of molecular interactions, enzymatic activities, and biological pathways, contributing to a better understanding of various biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 851916-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,1 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 851916-39:
(8*8)+(7*5)+(6*1)+(5*9)+(4*1)+(3*6)+(2*3)+(1*9)=187
187 % 10 = 7
So 851916-39-7 is a valid CAS Registry Number.

851916-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,4S)-4-(2,5-Dimethyl-1H-pyrrol-1-yl)-1-isopropyl-2-cyclopenten e-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names (1S-cis)-4-[2-AMino-6-(cyclopropylaMino)-9H-purin-9-yl]-2-cyclopentene-1-Methanol

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:851916-39-7 SDS

851916-39-7Downstream Products

851916-39-7Relevant academic research and scientific papers

AMINOCYCLOPENTYL PYRIDOPYRAZINONE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

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Page/Page column 40, (2010/11/27)

Compounds of Formula I and Formula II (wherein A, E, j, k, m, n, R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R15, R16, R17, R18, R19, R24, R25, R26, R27, R28, R29, R30, R31, R32, R33, R34, X, Y and Z are as defined herein) which are modulators of chemokine receptor activity and are useful in the prevention or treatment of certain inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which chemokine receptors are involved.

CCR-2 ANTAGONIST SALT

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Page/Page column 20, (2008/06/13)

The present invention provides an efficient synthesis for the preparation of ((1R,3S)-3-isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentyl)[(3S,4S)-3-m ethoxytetrahydro-2H-pyran-4-yl]amine and its succinate salt.

PROCESS FOR THE PREPARATION OF CCR-2 ANTAGONIST

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Page/Page column 7; 20, (2010/02/11)

The present invention provides an efficient synthesis for the preparation of ((1R,3S)-3-isopropyl-3- {[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl} cyclopentyl)[(3S,4S)-3-m ethoxytetrahydro- 2H-pyran-4-yl]amine and its succinate sal

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