24722-30-3 Usage
Description
Cyclohexanecarboxamidine, with the chemical formula C7H14N2, is a crystalline solid that plays a significant role in organic synthesis. It is utilized as a reagent for the preparation of a variety of compounds, including amino acids, pharmaceuticals, and agrochemicals. This versatile compound also serves as a building block for the synthesis of heterocyclic compounds and functions as a catalyst in numerous chemical reactions. Cyclohexanecarboxamidine is an essential intermediate in the production of quaternary ammonium compounds, which are extensively used as surfactants and disinfectants. Moreover, it has been investigated for its potential antifungal and antibacterial properties, highlighting its value in the realm of organic chemistry.
Uses
Used in Organic Synthesis:
Cyclohexanecarboxamidine is used as a reagent for the preparation of various compounds such as amino acids, pharmaceuticals, and agrochemicals. Its ability to participate in organic synthesis makes it a valuable component in the creation of a wide array of products.
Used in Heterocyclic Compound Synthesis:
CYCLOHEXANECARBOXAMIDINE is utilized as a building block in the synthesis of heterocyclic compounds, which are an important class of organic compounds with applications in various fields, including pharmaceuticals and materials science.
Used as a Catalyst:
Cyclohexanecarboxamidine functions as a catalyst in numerous chemical reactions, facilitating the progress of these reactions and improving their efficiency.
Used in the Production of Quaternary Ammonium Compounds:
As an important intermediate, cyclohexanecarboxamidine is crucial in the production of quaternary ammonium compounds. These compounds are widely used as surfactants and disinfectants, highlighting the compound's significance in various industries.
Used in Antimicrobial Applications:
Cyclohexanecarboxamidine has been studied for its potential antifungal and antibacterial properties, indicating its possible use in applications related to microbial control and sanitization.
Check Digit Verification of cas no
The CAS Registry Mumber 24722-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,2 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24722-30:
(7*2)+(6*4)+(5*7)+(4*2)+(3*2)+(2*3)+(1*0)=93
93 % 10 = 3
So 24722-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2.ClH/c8-7(9)6-4-2-1-3-5-6;/h6H,1-5H2,(H3,8,9);1H
24722-30-3Relevant articles and documents
Probing the effect of the amidinium group and the phenyl ring on the thermodynamics of binding of benzamidinium chloride to trypsin
Talhout, Reinskje,Engberts, Jan B.F.N.
, p. 3071 - 3074 (2004)
The effect of the amidinium group and the phenyl ring on the thermodynamics of binding of benzamidinium chloride to the serine proteinase trypsin has been studied using isothermal titration calorimetry. Binding studies with benzylammonium chloride, α-meth
PROCESS FOR PREPARING 5-FLUORO-1H-PYRAZOLO [3, 4-B] PYRIDIN-3-AMINE AND DERIVATIVES THEREOF
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Page/Page column 21; 38, (2009/03/07)
The present invention relates to a process for the synthesis of 5-fluoro-1H-pyrazolo [3, 4-b]pyridin-3-amine in high yield and purity. The present invention also relates to processes for the synthesis of 5-fluoro-1H-pyrazolo [3, 4- b] ρyridin-3-amine derivatives. These processes are useful for preparing biologically active compounds, particularly certain GSK-3 inhibitors, or derivatives thereof. Reagents and conditi ons : i. Pd ( OAc )2, PPh3, Et3N, H2CO2; i i. 1 ) (COCl )2, CH2Cl2, cat. DMF; 2 ) NH3 (g ), dioxane, i i i. TFAA, Et3N, CH2Cl2, O°C; iv. H2NNH2. H2O, n-butanol, reflux.
