90085-05-5

Basic information

• Product Name: Methyl 2-Hydroxycyclopentylcarboxylate
• Synonyms: methyl 2-hydroxycyclopentane-1-carboxylate;Cyclopentanecarboxylic acid, 2-hydroxy-, methyl ester;METHYL 2-HYDROXYCYCLOPENTANECARBOXYLATE（WS204748）
• CAS NO: 90085-05-5
• Molecular Formula: C₇H₁₂O₃
• Molecular Weight: 144.16838
• Mol File: 90085-05-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 212.1±33.0 °C(Predicted)
• Appearance: /
• Density: 1.169±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 14.60±0.40(Predicted)
• CAS DataBase Reference: Methyl 2-Hydroxycyclopentylcarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-Hydroxycyclopentylcarboxylate(90085-05-5)
• EPA Substance Registry System: Methyl 2-Hydroxycyclopentylcarboxylate(90085-05-5)

Safety Data

• Hazardous Substances Data: 90085-05-5(Hazardous Substances Data)

Usage

General Description

Methyl 2-Hydroxycyclopentylcarboxylate is a chemical compound that is commonly used in the production of fragrances and flavors. It is a clear, colorless liquid with a pleasant odor and is often employed as a fragrance ingredient in cosmetics, personal care products, and household items. Methyl 2-Hydroxycyclopentylcarboxylate is also utilized as a flavoring agent in the food industry, adding a sweet, fruity note to various food and beverage products. Methyl 2-Hydroxycyclopentylcarboxylate is produced synthetically and is considered safe for use in consumer products when used in accordance with regulatory guidelines.

Upstream product

• 10472-24-9 methyl 2-oxocyclopentane-1-carboxylate 
• 285-67-6 Cyclopentene oxide 
• 64-19-7 acetic acid 
• 186581-53-3 diazomethane 
• 81887-89-0 2-hydroxycyclopentyl-1-carboxylic acid 

Downstream Products

• 117959-75-8 <1α(R^*S^*),2α,2(E)>-(+/-)-2-(4,8-Dimethyl-3,7-nonadienyl)-2-(formyl)-α-<3-(phenylmethoxy)propyl>cyclopentaneacetaldehyde 
• 117959-73-6 <4aβ,7aβ(E)>-(+/-)-7a-(4,8-Dimethyl-3,7-nonadienyl)hexahydro-4-<3-(phenylmethoxy)propyl>cyclopentapyran-3(1H)-one 
• 117959-74-7 <1α(R^*S^*),2α,2(E)>-(+/-)-2-(4,8-Dimethyl-3,7-nonadienyl)-2-(hydroxymethyl)-β-<3-(phenylmethoxy)propyl>cyclopentaneethanol 
• 80969-64-8 <1R,2R>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 1,1-dimethylethyl ester 
• 81024-72-8 <1R,2S>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 1,1-dimethylethyl ester 
• 80969-61-5 <1S,2R>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 1,1-dimethylethyl ester 
• 81024-76-2 <1S,2S>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 1,1-dimethylethyl ester 
• 81024-77-3 <1R,2R>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 
• 81024-73-9 <1R,2S>-1-<2-(benzoylthio)cyclopentyl>carbonyl-L-proline 
• 81024-78-4 <1S,2S>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 
• 99397-53-2 cis-2-(benzoylthio)cyclopentanecarboxylic acid 
• 99343-54-1 trans-2-(benzoylthio)cyclopentanecarboxylic acid 
• 80969-62-6 <1S,2R>-1-<<2-(benzoylthio)cyclopentyl>carbonyl>-L-proline 
• 136788-13-1 N-<1-(2-naphthylthio)ethenyl>-N-(phenylmethyl)-1-cyclopentene-1-carboxamide 

Relevant articles and documents

MONOMER, POLYMER, RESIST COMPOSITION, AND PATTERNING PROCESS

A polymer for resist use is obtainable from a monomer having formula (1) wherein R1 is H, CH3 or CF3, R2 and R3 are a monovalent hydrocarbon group, R4 to R9 are hydrogen or a monovalent hydrocarbon group, R10 is a monovalent hydrocarbon group or fluorinat

Developing a Biocascade Process: Concurrent Ketone Reduction-Nitrile Hydrolysis of 2-Oxocycloalkanecarbonitriles

A stereoselective bioreduction of 2-oxocycloalkanecarbonitriles was concurrently coupled to a whole cell-catalyzed nitrile hydrolysis in one-pot. The first step, mediated by ketoreductases, involved a dynamic reductive kinetic resolution, which led to 2-hydroxycycloalkanenitriles in very high enantio- and diastereomeric ratios. Then, the simultaneous exposure to nitrile hydratase and amidase from whole cells of Rhodococcus rhodochrous provided the corresponding 2-hydroxycycloalkanecarboxylic acids with excellent overall yield and optical purity for the all-enzymatic cascade.

Non-Cp titanium alkoxide-based homolytic ring-opening of epoxides by an intramolecular hydrogen abstraction in β-titanoxy radical intermediates

A low-valent titanium species derived in situ from Ti(O-i-Pr)4, Me3SiCl and Mg powder in tetrahydrofuran reacted with epoxides to selectively provide less hindered alcohols via a homolytic ring-opening of epoxides, in which the intermediate β-titanoxy radical intramolecularly abstracted a hydrogen atom from an alkoxy moiety in the titanium complexes.