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1-cyanocyclobutanecarboxylic acid is a versatile chemical compound characterized by its cyclobutane ring structure, which is enriched with a cyanide group and a carboxylic acid group. This unique combination endows the molecule with special chemical properties, including the ability to act as a pharmacophore, allowing for optimal interaction with specific biological target structures. The carboxylic acid group also imparts acidic properties and enhances the compound's solubility in water, facilitating its use in a range of chemical reactions and modifications for the synthesis of pharmaceuticals and biologically active compounds.

30491-91-9

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30491-91-9 Usage

Uses

Used in Organic Chemistry:
1-cyanocyclobutanecarboxylic acid is used as a building block for the synthesis of various organic compounds due to its reactive cyclobutane ring and functional groups, which can be further modified to create a wide array of chemical entities.
Used in Medicinal Chemistry:
1-cyanocyclobutanecarboxylic acid is used as a key intermediate in the development of pharmaceuticals for its potential to be incorporated into drug molecules, enhancing their pharmacological properties and interactions with biological targets.
Used in Drug Design:
1-cyanocyclobutanecarboxylic acid is used as a pharmacophore in drug design for its ability to interact optimally with specific biological target structures, contributing to the development of more effective and selective therapeutic agents.
Used in Chemical Reactions:
1-cyanocyclobutanecarboxylic acid is used as a reactant in various chemical reactions due to its acidic properties and the reactivity of its cyclobutane ring and cyanide group, allowing for the formation of diverse chemical products.
Used in the Synthesis of Biologically Active Compounds:
1-cyanocyclobutanecarboxylic acid is used as a precursor in the synthesis of biologically active compounds, leveraging its structural features to create molecules with potential therapeutic or biological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30491-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,9 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30491-91:
(7*3)+(6*0)+(5*4)+(4*9)+(3*1)+(2*9)+(1*1)=99
99 % 10 = 9
So 30491-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2/c7-4-6(5(8)9)2-1-3-6/h1-3H2,(H,8,9)

30491-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyanocyclobutane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-cyano-1-cyclobutanecarboxylic acid

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:30491-91-9 SDS

30491-91-9Relevant academic research and scientific papers

6-(Substituted-cycloalkylcarboxamide) penicillanic acids

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, (2008/06/13)

Penicillins of the formula SPC1 Or a pharmaceutically-acceptable, nontoxic salt thereof, Wherein R1 and R2 are the same or different and each is hydrogen, fluorine, chlorine or bromine; or when R2 is hydrogen, R1 can also be cyano, hydroxyl, azido, amino or nitro; or R1 and R2 are bonded to a ring carbon atom and constitute a single oxygen atom; R3 is hydrogen, methyl, chlorine, bromine, cyano, methoxy or carboxyl; and n is 2 to 7; Are useful for their antibacterial activity.

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