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(1R,12S)-13-Oxabicyclo[10.1.0]tridecane is a complex organic compound with a unique cyclic structure. It is characterized by a 13-membered ring system that includes an oxygen atom, forming an oxa-bridge. The compound's stereochemistry is defined by the (1R,12S)-rel configuration, indicating the specific arrangement of atoms in three-dimensional space. This molecule is of interest in the field of organic chemistry, potentially for its structural properties or as a precursor in the synthesis of more complex molecules. It is important to note that the compound's specific applications, reactivity, and physical properties would depend on its detailed chemical context and the functional groups present.

1502-29-0

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1502-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1502-29-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1502-29:
(6*1)+(5*5)+(4*0)+(3*2)+(2*2)+(1*9)=50
50 % 10 = 0
So 1502-29-0 is a valid CAS Registry Number.

1502-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1,2-epoxycyclododecane

1.2 Other means of identification

Product number -
Other names cis-cyclododecane epoxide

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:1502-29-0 SDS

1502-29-0Relevant 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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