24722-30-3

Basic information

• Product Name: CYCLOHEXANECARBOXAMIDINE
• Synonyms: CYCLOHEXANECARBOXAMIDINE;CYCLOHEXANECARBOXAMIDINE HCL;Cyclohexanecarboxylic acid amidine;Hexahydrobenzamidine
• CAS NO: 24722-30-3
• Molecular Formula: C₇H₁₄N₂
• Molecular Weight: 126.2
• Product Categories: pharmacetical
• Mol File: 24722-30-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 204.9 °C at 760 mmHg
• Flash Point: 77.7 °C
• Appearance: /
• Density: 1.14 g/cm³
• Vapor Pressure: 0.023mmHg at 25°C
• CAS DataBase Reference: CYCLOHEXANECARBOXAMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOHEXANECARBOXAMIDINE(24722-30-3)
• EPA Substance Registry System: CYCLOHEXANECARBOXAMIDINE(24722-30-3)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 24722-30-3(Hazardous Substances Data)

Usage

General Description

Cyclohexanecarboxamidine is a chemical compound with the formula C7H14N2. It is a crystalline solid that is commonly used in organic synthesis as a reagent for the preparation of various compounds, such as amino acids, pharmaceuticals, and agrochemicals. Cyclohexanecarboxamidine is also used as a building block for the synthesis of heterocyclic compounds and as a catalyst in various chemical reactions. It is an important intermediate in the production of quaternary ammonium compounds, which are widely used as surfactants and disinfectants. Additionally, cyclohexanecarboxamidine has been studied for its potential antifungal and antibacterial properties, making it a versatile and valuable chemical in the field of organic chemistry.

InChI:InChI=1/C7H14N2.ClH/c8-7(9)6-4-2-1-3-5-6;/h6H,1-5H2,(H3,8,9);1H

Upstream product

• 94052-40-1 methyl cyclohexanecarboximidate hydrochloride 
• 166985-85-9 N-phenylcyclohexanecarboximidamide 
• 7664-41-7 ammonia 
• 100-61-8 N-methylaniline 
• 766-05-2 cyclohexane carbonitrile 

Downstream Products

• 681178-94-9 5-(4-chloro-phenyl)-3-(2-cyclohexyl-3H-imidazol-4-yl)-1-(2,4-dichloro-phenyl)-4-methyl-1H-pyrazole 
• 1436594-20-5 5-chloro-2-cyclohexylpyrimidine 
• 1423042-49-2 5-chloro-3-cyclohexyl-[1,2,4]thiadiazole 
• 1423042-30-1 1-(3-cyclohexyl-[1,2,4]thiadiazol-5-yl)-4-[2-(4-methoxyphenyl)ethyl]piperazine 
• 94052-11-6 2,6-dichloro-2-cyclohexylpyrimidine 
• 93624-52-3 1,5-dicyclohexylimidazol 
• 55041-14-0 2-(cyclohexyl)-4,5-diphenyl-1H-imidazole 
• 111114-70-6 2-cyclohexyl-4-phenyl-1H-imidazole 

Relevant articles and documents

Probing the effect of the amidinium group and the phenyl ring on the thermodynamics of binding of benzamidinium chloride to trypsin

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

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.