1776-53-0

Basic information

• Product Name: 4-AMINOCYCLOHEXANECARBOXYLIC ACID
• Synonyms: CYCLOHEXANECARBOXYLIC ACID, 4-AMINO-;4-AMINOHEXAHYDROBENZOIC ACID;4-AMINOCYCLOHEXANECARBOXYLIC ACID;4-Aminocyclohexanecarboxylic acidcis/trans mixture;AMINOCYCLOHEXANECARBOXYLIC ACID;AKOS BB-9763;4-Aminocyclohexylcarboxylic Acid;P-AMINOCYCLOHEXYLCARBOXYLIC ACID
• CAS NO: 1776-53-0
• Molecular Formula: C₇H₁₃NO₂
• Molecular Weight: 143.18
• EINECS: 1592732-453-0
• Product Categories: 4-Substituted Cyclohexanecarboxylic Acids;Bifunctional Compounds (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials
• Mol File: 1776-53-0.mol
• Article Data: 17

Chemical Properties

• Melting Point: 299-301 ºC
• Boiling Point: 280°C at 760 mmHg
• Flash Point: 123.1°C
• Appearance: /
• Density: 1.133g/cm³
• Vapor Pressure: 0.00103mmHg at 25°C
• Refractive Index: 1.503
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.46±0.10(Predicted)
• Water Solubility: almost transparency
• CAS DataBase Reference: 4-AMINOCYCLOHEXANECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINOCYCLOHEXANECARBOXYLIC ACID(1776-53-0)
• EPA Substance Registry System: 4-AMINOCYCLOHEXANECARBOXYLIC ACID(1776-53-0)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-41-37/38-22
• Safety Statements: 26-36/37/39-36-39
• Hazardous Substances Data: 1776-53-0(Hazardous Substances Data)

Usage

General Description

4-Aminocyclohexanecarboxylic acid is a chemical compound with the molecular formula C7H13NO2. It is a cyclic amino acid that contains a cyclohexane ring and an amino group attached to the carbon of its carboxylic acid group. 4-AMINOCYCLOHEXANECARBOXYLIC ACID has potential applications in the pharmaceutical industry, where it can be used as a building block for the synthesis of various drugs and pharmaceutical compounds. Its structure and properties make it a useful intermediate for the production of diverse medicinal products. Additionally, 4-aminocyclohexanecarboxylic acid may also have potential biological and pharmacological activities, making it a subject of interest for further research and development.

InChI:InChI=1/C7H13NO2/c8-6-3-1-5(2-4-6)7(9)10/h5-6H,1-4,8H2,(H,9,10)

Upstream product

• 90942-89-5 ethyl 4-(hydroxyimino)cyclohexane-1-carboxylate 
• 150-13-0 4-amino-benzoic acid 
• 7732-18-5 water 
• 71-41-0 pentan-1-ol 
• 17159-79-4 ethyl 4-oxocyclohexane-1-carboxylate 
• 6297-22-9 4-carbomethoxycyclohexanone 
• 38446-95-6 4-oxocyclohexanecarboxylic acid tert-butyl ester 
• 57555-71-2 4-hydroxyimino-cyclohexanecarboxylic acid 

Downstream Products

• 804548-16-1 methyl trans-4-[[(4-methoxy-2,3,6-trimethylphenyl)sulfonyl]amino]cyclohexanecarboxylate 
• 189504-64-1 4-But-3-enoylamino-cyclohexanecarboxylic acid 
• 130309-46-5 trans-4-(tert-butoxycarbonylamino)cyclohexane carboxylic acid 
• 102390-35-2 trans-4-(trifluoroacetamido)cyclohexanecarboxylic acid 
• 147900-46-7 trans-4-(fluorenylmethoxycarbonylamino)cyclohexanecarboxylic acid 
• 3306-69-2 2-azabicyclo-<2,2,2>-octa-3-one 
• 105562-49-0 4-Isocyanatocyclohexancarbonylchlorid 
• 175867-59-1 methyl 4-aminocyclohexane-1-carboxylate 
• 1678-68-8 ethyl trans-4-aminocyclohexanecarboxylate 
• 62456-15-9 methyl trans-4-amino-cyclohexanecarboxylate 
• 102390-34-1 trans-4-acetamidocyclohexanecarboxylic acid 
• 3306-69-2 2-aza-bicyclo[2.2.2]octan-3-one 
• 51498-33-0 ethyl 4-amino-1-cyclohexanecarboxylate 
• 34771-04-5 (1r,4r)-4-(((benzyloxy)carbonyl)amino)cyclohexane carboxylic acid 

Relevant articles and documents

NMR AND RAMAN SPECTROSCOPIC STUDY OF COMPLEX FORMATION BETWEEN 2-METHYL-2-AZABICYCLO--OCTA-3-ONE AND TiCl4

From analysis of 1H and 13C NMR and Raman specroscopic data, in CDCl3 and 1,1,2,2-tetrachloroethane-d2 solution, the lactam 2-methyl-2-azabicyclo--octa-3-one (L) was found to form complexes with TiCl4 (M) of overall composition M2/

Preparation method of trans 4 - (tert-butyloxycarbonylamino) cyclohexanecarboxylic acid and intermediate thereof

The invention provides a preparation method of trans 4 - (tert-butyloxycarbonylamino) cyclohexanecarboxylic acid and an intermediate thereof. The preparation method is characterized by comprising the following steps of 4 - oxocyclohexane carboxylic ester and chiral ligand reagent tert-butyl sulfinamide as a raw material, reducing amination to obtain trans -4 -tert-butyl sulfinyl sulfenamide cyclohexane carboxylic acid ester by virtue of chiral ligand reagent tert-butyl sulfinamide and 4 - 95% -oxocyclohexane carboxylic ester, and is stable in basic conditions and easy to leave under an acidic condition. Reaction conditions are mild, operation is simple and convenient, yield is high, and industrial production is easy.

Upgrading of aromatic compounds in bio-oil over ultrathin graphene encapsulated Ru nanoparticles

Fast pyrolysis of biomass for bio-oil production is a direct route to renewable liquid fuels, but raw bio-oil must be upgraded in order to remove easily polymerized compounds (such as phenols and furfurals). Herein, a synthesis strategy for graphene encapsulated Ru nanoparticles (NPs) on carbon sheets (denoted as Ru@G-CS) and their excellent performance for the upgrading of raw bio-oil were reported. Ru@G-CS composites were prepared via the direct pyrolysis of mixed glucose, melamine and RuCl3 at varied temperatures (500-800 °C). Characterization indicated that very fine Ru NPs (2.5 ± 1.0 nm) that were encapsulated within 1-2 layered N-doped graphene were fabricated on N-doped carbon sheets (CS) in Ru@G-CS-700 (pyrolysis at 700 °C). And the Ru@G-CS-700 composite was highly active and stable for hydrogenation of unstable components in bio-oil (31 samples including phenols, furfurals and aromatics) even in aqueous media under mild conditions. This work provides a new protocol to the utilization of biomass, especially for the upgrading of bio-oil.

NOVEL MULTIMERIC CD40 LIGANDS, METHOD FOR PREPARING SAME AND USE THEREOF FOR PREPARING DRUGS

The invention concerns a compound of formula (I), wherein Y represents a macrocycle whereof the cycle comprises 9 to 36 atoms, and is functionalized by three amine or COOH functions; Rc represents a group of formula H—Xa—Xb—Xc—Xd—Xe—(Xf)i—, wherein i represents 0 or 1, Xn is in particular selected among lysine, arginine, ornithine residues, Xb is in particular selected among glycine, asparagine, L-proline or D-proline residues, Xc et Xd are in particular selected among tyrosine, phenylalanine or 3-nitrotyrosine residues, Xe et Xf are in particular selected among the following amino acid residues: NH2—(CH2)n—COOH, n ranging from 1 to 10 or NH2—(CH2—CH2—O)m—CH2CH2COOH, m ranging from 3 to 6, provided that one at least of the amino acid residues Xa, Xb, Xc and Xd is different from the corresponding amino acid in the sequence of the natural CD40 143Lys-Gly-Tyr-Tyr146 fragment