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2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester is a complex chemical compound with a unique structure. It features a cyclohexene ring, a carboxylic acid group, a 2-hydroxy-4-oxo-6-pentyl moiety, and a methyl ester functional group. This combination of functional groups suggests its potential use in various chemical reactions and as a precursor in the synthesis of other compounds.

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  • 2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester

    Cas No: 27871-89-2

  • USD $ 1.9-2.9 / Gram

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  • 27871-89-2 Structure
  • Basic information

    1. Product Name: 2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester
    2. Synonyms: methyl 2-hydroxy-4-oxo-6-pentyl-2-cyclohexene-1-carboxylate;CYC075;2-Cyclohexene-1-carboxylic acid,2-hydroxy-4-oxo-6-pentyl-,methyl ester;
    3. CAS NO:27871-89-2
    4. Molecular Formula: C13H20O4
    5. Molecular Weight: 240.299
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27871-89-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 349.2±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.112±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester(27871-89-2)
    11. EPA Substance Registry System: 2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester(27871-89-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 27871-89-2(Hazardous Substances Data)

27871-89-2 Usage

Uses

Used in Organic Synthesis:
2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester is used as a precursor in organic synthesis for the production of other compounds. Its complex structure and various functional groups make it a versatile building block for creating more complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and functional groups can be utilized to create new drugs or improve the properties of existing ones.
Used in Chemical Manufacturing:
2-Cyclohexene-1-carboxylic acid, 2-hydroxy-4-oxo-6-pentyl-, methyl ester is also used in chemical manufacturing as a raw material for the production of various chemical products. Its potential applications in this field include the synthesis of specialty chemicals, polymers, and other materials.

Check Digit Verification of cas no

The CAS Registry Mumber 27871-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,7 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27871-89:
(7*2)+(6*7)+(5*8)+(4*7)+(3*1)+(2*8)+(1*9)=152
152 % 10 = 2
So 27871-89-2 is a valid CAS Registry Number.

27871-89-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-hydroxy-4-oxo-6-pentylcyclohex-2-ene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Cyclohexene-1-carboxylic acid,2-hydroxy-4-oxo-6-pentyl-,methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27871-89-2 SDS

27871-89-2Downstream Products

27871-89-2Relevant articles and documents

BIOENZYMATIC SYNTHESIS OF THC-v, CBV AND CBN AND THEIR USE AS THERAPEUTIC AGENTS

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Paragraph 0124; 0125, (2017/10/18)

The present invention provides methods for producing cannabinoids. More specifically, the invention is directed to the bio-enzymatic synthesis of THC-v, CBV and CBN by contacting a compound according to Formula I with a cannabinoid synthase enzyme. Also described is a system for producing these pharmaceutically important cannabinoids and the use of such cannabinoids as therapeutic agents.

BIOSYNTHESIS OF CANNABINOID PRODRUGS AND THEIR USE AS THERAPEUTIC AGENTS

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Paragraph 0187; 0188, (2017/11/07)

The present invention provides methods for producing cannabinoid prodrugs. Also described are pharmaceuticals acceptable compositions of the prodrugs and a system for the large-scale production of the prodrugs.

METHODS FOR THE MANUFACTURE OF CANNABINOID PRODRUGS, PHARMACEUTICAL FORMULATIONS AND THEIR USE

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Paragraph 0131; 0132, (2018/01/18)

Described are methods for producing cannabinoid prodrugs as well as methods for formulating such prodrugs in a pharmaceutically acceptable form and their use as therapeutic agents for treating diseases.

APPARATUS AND METHODS FOR THE SIMULTANEOUS PRODUCTION OF CANNABINOID COMPOUNDS

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Page/Page column 66, (2016/03/22)

The present invention provides an apparatus and methods for simultaneously producing different compounds in various ratios under set conditions.

BIOSYNTHESIS OF CANNABINOIDS

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Paragraph 0119, (2014/09/16)

The present invention provides methods for producing cannabinoids and cannabinoid analogs as well as a system for producing these compounds. The inventive method is directed to contacting a compound according to Formula I or Formula II with a cannabinoid synthase. Also described is a system for producing cannabinoids and cannabinoid analogs by contacting a THCA synthase with a cannabinoid precursor and modifying at least one property of the reaction mixture to influence the quantity formed of a first cannabinoid relative to the quantity formed of a second cannabinoid.

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