6149-50-4

Basic information

• Product Name: methyl 1-hydroxycyclohexane-1-carboxylate
• Synonyms: methyl 1-hydroxycyclohexane-1-carboxylate;1-Hydroxy-cyclohexanecarboxylic acid methyl ester
• CAS NO: 6149-50-4
• Molecular Formula: C₈H₁₄O₃
• Molecular Weight: 158.2
• Mol File: 6149-50-4.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 208°C at 760 mmHg
• Flash Point: 78.1°C
• Appearance: /
• Density: 1.134g/cm³
• Vapor Pressure: 0.0507mmHg at 25°C
• Refractive Index: 1.486
• CAS DataBase Reference: methyl 1-hydroxycyclohexane-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 1-hydroxycyclohexane-1-carboxylate(6149-50-4)
• EPA Substance Registry System: methyl 1-hydroxycyclohexane-1-carboxylate(6149-50-4)

Safety Data

• Hazardous Substances Data: 6149-50-4(Hazardous Substances Data)

Usage

General Description

Methyl 1-hydroxycyclohexane-1-carboxylate is a chemical compound with the molecular formula C8H12O3. It is commonly used as a flavor and fragrance ingredient due to its fruity and floral odor. This chemical is a colorless liquid with a mild, sweet flavor, making it a popular choice for use in food and beverage products. Additionally, methyl 1-hydroxycyclohexane-1-carboxylate is also used in the production of various personal care products and as a solvent in different industrial applications. It is important to handle this chemical with care and follow safety guidelines due to its potential for irritation and toxicity if exposure occurs.

InChI:InChI=1/C8H14O3/c1-11-7(9)8(10)5-3-2-4-6-8/h10H,2-6H2,1H3

Upstream product

• 40195-26-4 1-methoxy-1-trimethylsilyloxymethylenecyclohexane 
• 108-94-1 cyclohexanone 
• 67-56-1 methanol 
• 931-97-5 1-hydroxy-1-cyclohexanecarbonitrile 
• 24731-36-0 1-trimethylsilanyloxycyclohexanecarbonitrile 
• 138723-92-9 2,2-dimethoxy-5,5-pentamethylene-1,3,4-Δ³-oxadiazoline 
• 186581-53-3 diazomethane 
• 98-89-5 Cyclohexanecarboxylic acid 
• 7500-69-8 1-hydroxycyclohexanecarboxamide 
• 1123-28-0 1-hydroxy-cyclohexanecarboxylic acid 

Downstream Products

• 855600-18-9 1-acetoacetyloxy-cyclohexanecarboxylic acid methyl ester 
• 76718-04-2 3-Benzoylmethylen-2,2-pentamethylen-5-phenyl-2,3-dihydrofuran 
• 76718-05-3 3-(4-Chlorbenzoyl)methylen-5-(4-chlorphenyl)-2,2-pentamethylen-2,3-dihydrofuran 
• 98-89-5 Cyclohexanecarboxylic acid 
• 22884-78-2 1-oxa-spiro[4.5]decane-2,4-dione 
• 22884-85-1 3-acetyl-1-oxa-spiro[4.5]decane-2,4-dione 
• 1101271-49-1 4-hydroxy-3-(4-methoxyphenyl)-1-oxaspiro[4.5]dec-3-en-2-one 
• 1396787-19-1 2-benzylidene-1-oxaspiro[3.5]nonan-3-one 
• 1396787-38-4 2-benzylidene-1-oxaspiro[3.5]nonan-3-one 
• 1396787-20-4 2-(4-methoxybenzylidene)-1-oxaspiro[3.5]nonan-3-one 
• 1396787-40-8 2-(4-methoxybenzylidene)-1-oxaspiro[3.5]nonan-3-one 
• 1396787-21-5 2-(4-chlorobenzylidene)-1-oxaspiro[3.5]nonan-3-one 
• 1396787-41-9 2-(4-chlorobenzylidene)-1-oxaspiro[3.5]nonan-3-one 
• 1396787-53-3 methyl 1-[(dimethoxyphosphoryl)methoxy]cyclohexanecarboxylate 

Relevant articles and documents

Synthesis method 2- hydroxyl carboxylic ester (by machine translation)

The method, is simple 2 - energy consumption, energy consumption is low, the production :(1) of waste water can be greatly reduced, the yield of the target product is high 2 - and the production cost ;(2) is greatly reduced (1). 2 - The method comprises the following steps, preparing 2 - hydroxycarboxylate, with an acid ;(3) by a byproduct ammonium salt (2) in step, and filtering the excess acid, to remove the byproduct ammonium salt, to obtain 2 - hydroxyl carboxylic acid ester product, by esterification reaction in step (, and filtering to remove 2 - the excess, alcohol), from, the reaction, solution obtained by the reaction solution; of the catalyst under the, action of, a catalyst, to obtain the product of the compound. (by machine translation)

Anesthetic compounds and related methods of use

Provided herein are compounds according to formula (I): Provided herein is also a pharmaceutical composition comprising a compound according to formula (I) and a pharmaceutically acceptable carrier, and a method for providing anesthesia in a subject by administering such a pharmaceutical composition.

Method for the efficient synthesis of highly-substituted oxetan- and azetidin-, dihydrofuran- and pyrrolidin-3-ones and its application to the synthesis of (±)-pseudodeflectusin

Highly substituted four- and five-membered heterocycles were prepared starting with O,P- and N,P-acetals by using a one-pot method involving base induced cyclization and a Horner-Wadsworth-Emmons (HWE) olefination reaction. Divergent synthesis of various heterocycles was achieved by using this method and transformations of the alkenyl group in the products of these processes were exemplified. Finally, a short and efficient synthesis of (±)- pseudodeflectusin based on the new methodology was achieved.