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2-Diisobutylcarbamoyl-cyclohexanecarboxylic acid is a chemical compound derived from cyclohexanecarboxylic acid, featuring a diisobutylcarbamoyl group. 2-DIISOBUTYLCARBAMOYL-CYCLOHEXANECARBOXYLIC ACID exhibits potential bioactivity and possesses properties that make it a promising candidate for pharmaceutical drug development. Its unique structure and chemical properties are of interest for further research and development in the pharmaceutical industry.

332394-38-4

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332394-38-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Diisobutylcarbamoyl-cyclohexanecarboxylic acid is used as a potential drug candidate for its bioactivity and properties that may contribute to the development of new pharmaceutical drugs. Its unique structure and chemical properties make it a valuable compound for research and development in the pharmaceutical field.
Used in Drug Development:
2-Diisobutylcarbamoyl-cyclohexanecarboxylic acid is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its potential bioactivity and chemical properties allow it to be a valuable component in the creation of new drugs with specific therapeutic effects.
Used in Medicinal Chemistry Research:
2-Diisobutylcarbamoyl-cyclohexanecarboxylic acid is used as a research tool in medicinal chemistry to study its interactions with biological targets and to understand its potential therapeutic effects. Its unique structure and properties provide insights into the design and optimization of new drug candidates.

Check Digit Verification of cas no

The CAS Registry Mumber 332394-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,3,9 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 332394-38:
(8*3)+(7*3)+(6*2)+(5*3)+(4*9)+(3*4)+(2*3)+(1*8)=134
134 % 10 = 4
So 332394-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H29NO3/c1-11(2)9-17(10-12(3)4)15(18)13-7-5-6-8-14(13)16(19)20/h11-14H,5-10H2,1-4H3,(H,19,20)/p-1/t13-,14-/m1/s1

332394-38-4SDS

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 2-[bis(2-methylpropyl)carbamoyl]cyclohexane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Diisobutylcarbamoyl-cyclohexanecarboxylic 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:332394-38-4 SDS

332394-38-4Downstream Products

332394-38-4Relevant academic research and scientific papers

Bestimmung von Stabilitaetskonstanten in Ethanol fuer Li+-selektive Ionophore mittels differentieller Dampfdruckosmometrie

Bliggensdorfer, Rene von,Suter, Gabriela,Simon, Wilhelm

, p. 1164 - 1170 (1989)

Stability constants of some neutral carriers and their bridged isologues in interaction with Li+ and Na+ are determined by a differential vapour pressure osmometry method in ethanol utilizing Bjerrum formation curves.All ionophores studied induce high Li+ selectivity in solvent polymeric membranes.

Lipophilic Diamides as Ionophores for Alkali and Alkaline Earth Metal Cations

Erne, Daniel,Ammann, Daniel,Zhukov, Alex F.,Behm, Felix,Pretsch, Ernoe,Simon, Wilhelm

, p. 538 - 545 (2007/10/02)

A sries of lipophilic N,N,N',N'-tetrasubstituted diamides were prepared and their selectivity in solvent polymeric membranes was studied. cis-N,N,N',N'-Tetraisobutylcyclohexane-1,2-dicarboxamide includes a selectivity in membranes for Li+ over alkaline earth metal cations and other alkali metal cations by a factor of about 1000 and 100 respectively.The ionophore N,N'-diheptyl-N,N'-dimethylethylmalonamide is an attractive candidate for the use in microelectrodes for the determination of intracellular Mg2+-activities.

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