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13-Oxabicyclo[10.1.0]tridecane, (1R,12R)-rel-, also known as (1R,12R)-13-Oxabicyclo[10.1.0]tridecane, is a complex organic compound with the molecular formula C13H24O. It features a unique bicyclic structure with a three-membered ring and a ten-membered ring, connected by an oxygen atom. The compound has two chiral centers at the 1st and 12th carbon atoms, with the R configuration at both positions. This specific stereochemistry is crucial for its properties and potential applications. The compound is of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals or other specialty chemicals.

4683-60-7

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4683-60-7 Usage

Chemical structure

A bicyclic compound derived from bicyclo[10.1.0]tridecane with an oxygen atom inserted into the carbon ring.

Chirality

The compound is chiral, meaning it has a non-superimposable mirror image.

Stereochemistry

The (1R,12R)-relconfiguration indicates the absolute stereochemistry of the molecule, describing the spatial arrangement of atoms in the compound.

Potential applications

The compound has potential applications in organic synthesis and material science.

Research interest

Its unique structure makes it of interest to researchers in the field of chemical and pharmaceutical sciences.

Further studies

Additional research may reveal the compound's potential pharmaceutical and industrial uses.

Molecular weight

Approximately 196.33 g/mol (calculated from the molecular formula).

Physical state

Likely a solid at room temperature, given its molecular weight and structure.

Solubility

The compound's solubility properties are not provided, but it may be soluble in organic solvents such as ethanol, methanol, or dichloromethane.

Stability

Information on the compound's stability is not provided, but it may be sensitive to heat, light, or moisture, as is common with many organic compounds.

Synthesis

The synthesis of 13-Oxabicyclo[10.1.0]tridecane, (1R,12R)-relis not described in the material provided, but it likely involves the introduction of an oxygen atom into the carbon ring of bicyclo[10.1.0]tridecane.

Derivatives

The compound is a derivative of bicyclo[10.1.0]tridecane, which may have different properties and applications.

Nomenclature

The compound's name follows the IUPAC nomenclature rules, indicating its structure and stereochemistry.

Hazards

Information on potential hazards, such as toxicity or reactivity, is not provided in the material. However, it is essential to consider these factors when handling and studying new chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 4683-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4683-60:
(6*4)+(5*6)+(4*8)+(3*3)+(2*6)+(1*0)=107
107 % 10 = 7
So 4683-60-7 is a valid CAS Registry Number.

4683-60-7SDS

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 trans-1,2-epoxycyclododecane

1.2 Other means of identification

Product number -
Other names -

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:4683-60-7 SDS

4683-60-7Relevant academic research and scientific papers

PROCESS FOR PREPARATION OF CYCLODODECANONE

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Page 8-9, (2008/06/13)

In the process for producing a cyclododecanone by iscmerizing an epoxycyclododecane-containing starting material in the presence of an isomerization reaction catalyst containing lithium bromide and/or lithium iodide, in order to perform the reaction with high efficiency (high reaction rate) and high selectivity and stably produce a high-purity cyclododecanone in industry while maintaining a high-level reaction rate, the epoxycyclododecane-containing starting material is produced by contacting an epoxycyclododecadiene with hydrogen in the presence of a hydrogen-reduction catalyst and has a content of the hydroxyl group-containing cyclododecane compounds contained in the epoxycyclododecane-containing starting material controlled to 5 mol% or less.

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