343775-23-5

Basic information

• Product Name: ethyl 2-(4-aMinocyclohexyl)acetate
• Synonyms: ethyl 2-(4-aMinocyclohexyl)acetate;ethyl 2-(4-aMinocyclohexyl)acetate-27;4-Aminocyclohexaneacetic acid ethyl ester HCl
• CAS NO: 343775-23-5
• Molecular Formula: C₁₀H₁₉NO₂
• Molecular Weight: 185.26336
• Mol File: 343775-23-5.mol

Chemical Properties

• Boiling Point: 253.2°C at 760 mmHg
• Flash Point: 116.8°C
• Appearance: /
• Density: 0.984g/cm³
• Vapor Pressure: 0.0185mmHg at 25°C
• Refractive Index: 1.46
• CAS DataBase Reference: ethyl 2-(4-aMinocyclohexyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(4-aMinocyclohexyl)acetate(343775-23-5)
• EPA Substance Registry System: ethyl 2-(4-aMinocyclohexyl)acetate(343775-23-5)

Safety Data

• Hazardous Substances Data: 343775-23-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 2-(4-aminocyclohexyl)acetate is used as a chemical intermediate for the synthesis of various pharmaceutical drugs, contributing to the development of new medications and therapies.
Used in Food Industry:
In the food industry, ethyl 2-(4-aminocyclohexyl)acetate is utilized as a flavoring agent, enhancing the aromatic and fruity notes in food products to improve taste and consumer appeal.
Used in Fragrance Production:
Ethyl 2-(4-aminocyclohexyl)acetate is employed in the production of fragrances, where its distinct scent characteristics are incorporated into perfumes, cosmetics, and other scented products to create desirable olfactory experiences.
Used in Organic Synthesis and Medicinal Chemistry:
ethyl 2-(4-aMinocyclohexyl)acetate may also have potential applications in the fields of organic synthesis and medicinal chemistry, where it could be used to create new chemical entities or improve existing synthesis processes for pharmaceuticals and other chemical products.

InChI:InChI=1/C10H19NO2/c1-2-13-10(12)7-8-3-5-9(11)6-4-8/h8-9H,2-7,11H2,1H3

Downstream Products

• 2952-00-3 trans-2-(4-aminocyclohexyl)acetic acid 

Relevant articles and documents

Preparation method of 2-(4-aminocyclohexyl)-ethyl acetate

The invention provides a preparation method of 2-(4-aminocyclohexyl)-ethyl acetate, and belongs to the field of pharmaceutical chemistry. According to the preparation method, 1, 4-cyclohexanedione istaken as an initial raw material, and Wittig reaction, condensation reaction, catalytic hydrogenation, and the like are carried out so as to obtain 2-(4-aminocyclohexyl)-ethyl acetate. The purity of obtained 2-(4-aminocyclohexyl)-ethyl acetate is high; it is beneficial for preparation of dopamine receptor ligand drugs; the raw materials are widely available; operation is simple; reaction conditions are mild; and industrial application prospect is promising.

Novel thiophene derivatives, their process of preparation and the pharmaceutical compositions which comprise them

A compound of formula (I) selected from: wherein: X represents oxygen or sulphur, Y represents oxygen, —NH— or —N(C1-C6)alkyl-, Ra represents hydrogen, halogen, (C1-C3)alkyl, hydroxyl or (C1-C3)alkoxy, Rb represents hydrogen, halogen or (C1-C3)alkyl, A represents phenyl, pyridyl, (C5-C6)cycloalkyl or (C5-C6)cycloalkenyl, R1 and R2 each represent a group selected from hydrogen, halogen, cyano, nitro, haloalkyl, haloalkoxy, alkyl, alkenyl, alkynyl, —OR4, —NR4R5, —S(O)nR4, —C(O)R4, —CO2R4, —O—C(O)R4, —C(O)NR4R5, —NR5—C(O)R4, —NR5—SO2R4, -T-CN, -T-OR4, -T-OCF3, -T- NR4R5, -T-S(O)nR4, -T-C(O)R4, -T-CO2R4, -T-O—C(O)R4, -T-C(O)NR4R5, -T-NR4—C(O)R5, -T-NR4—SO2R5, —R6 and -T-R6 in which n, T, R4, R5 and R6 are as defined in the description, R3 represents an —R7 or —U—R11 group in which R7 represents hydrogen, alkyl, aryl, cycloalkyl or heterocycle, U represents a linear or branched alkylene chain and R11 is defined in the description, their optical isomers or their addition salts with a pharmaceutically acceptable acid or base, and their use as inhibitor of metalloproteinase and more specifically of metalloproteinase-12.