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1-(phenylsulfonyl)cyclopentanecarbonitrile, with the molecular formula C13H11NO2S, is a cyclopentylcarbonitrile derivative featuring a phenylsulfonyl group. This chemical compound is recognized for its versatile reactivity and potential applications in medicinal chemistry, making it a valuable building block in organic synthesis and pharmaceutical research. Its unique structural and reactivity features have also attracted attention in the field of organic chemistry, particularly in the development of new methods for carbon-carbon bond formation.

170803-75-5

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170803-75-5 Usage

Uses

Used in Pharmaceutical Research:
1-(phenylsulfonyl)cyclopentanecarbonitrile is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new pharmaceuticals. Its potential pharmacological properties make it a promising candidate for creating novel drugs with improved efficacy and reduced side effects.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(phenylsulfonyl)cyclopentanecarbonitrile serves as a key intermediate for the creation of complex molecular structures. Its unique reactivity allows for the formation of carbon-carbon bonds, which are essential in constructing a wide range of organic compounds.
Used in Medicinal Chemistry:
1-(phenylsulfonyl)cyclopentanecarbonitrile is utilized as a versatile starting material in medicinal chemistry, enabling the design and synthesis of new drug candidates with potential therapeutic applications. Its structural diversity and reactivity make it an attractive option for researchers seeking to develop innovative treatments for various diseases and conditions.
Used in Carbon-Carbon Bond Formation:
1-(phenylsulfonyl)cyclopentanecarbonitrile plays a significant role in the development of new methods for carbon-carbon bond formation, a critical aspect of organic chemistry. Its unique structural features facilitate the creation of these bonds, which are essential for constructing complex organic molecules and advancing the field of chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 170803-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,8,0 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 170803-75:
(8*1)+(7*7)+(6*0)+(5*8)+(4*0)+(3*3)+(2*7)+(1*5)=125
125 % 10 = 5
So 170803-75-5 is a valid CAS Registry Number.

170803-75-5SDS

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 1-(phenylsulfonyl)cyclopentanecarbonitrile

1.2 Other means of identification

Product number -
Other names 1-benzenesulphonyl-cyclopentanecarbonitrile

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:170803-75-5 SDS

170803-75-5Relevant academic research and scientific papers

Two-Carbon Elongation/Annulation of Alcohols to Nitriles

Lai, Jing-Yu,Yu, Jurong,Hawkins, R. David,Falck, J. R.

, p. 5691 - 5694 (1995)

Alcohols were replaced by a two-carbon nitrile unit in good to excellent yields via dehydrative alkylation with (phenylsulfonyl)acetonitrile under modified Mitsunobu conditions followed by desulfonylation using magnesium.Diols and haloalcohols furnished cycloalkylnitriles.

NOVEL DERIVATIVES OF PHENYLUREAS, INHIBITORS OF THE SOAT-1 ENZYME, PHARMACEUTICAL AND COSMETIC COMPOSITIONS CONTAINING THEM

-

Page/Page column 19-20, (2009/04/25)

The present invention relates to compounds of formula (I) : as well as to cosmetic and pharmaceutical compositions containing such a compound.

SYNTHESIS OF THE NITRILES AND AMIDES OF 1-(ARYLSULFONYL)CYCLOALKANESCARBOXYLIC ACIDS

Neplyuev, V. M.,Bazavova, I. M.,Esipenko, A. N.,Lozinskii, M. O.

, p. 1712 - 1716 (2007/10/02)

1-Arylsulfonylcycloalkanecarbonitriles were synthesized by the cycloalkylation of arylsulfonylacetonitriles by terminal dihalogenoalkanes under the conditions of phase-transfeer catalysis.Hydrolysis of the products gave 11-arylsulfonylcycloalkanecarboxyli

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