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Oxepino[4,5-c]pyridine is a heterocyclic compound characterized by a unique structure that combines a pyridine ring with an oxepine ring. Oxepino4,5-cpyridine is notable for its potential applications in medicinal chemistry and material science due to its diverse chemical properties. The fusion of these two rings creates a stable and rigid framework that can interact with various biological targets, making it a promising candidate for the development of new drugs. Additionally, its electronic and steric properties can be fine-tuned through substitution, which allows for the exploration of its potential in creating new materials with specific properties. The synthesis and study of oxepino[4,5-c]pyridine derivatives are areas of active research, with the aim of uncovering their full potential in various fields.

264-33-5

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264-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 264-33-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 264-33:
(5*2)+(4*6)+(3*4)+(2*3)+(1*3)=55
55 % 10 = 5
So 264-33-5 is a valid CAS Registry Number.

264-33-5SDS

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 oxepino[4,5-c]pyridine

1.2 Other means of identification

Product number -
Other names Oxepino4,5-cpyridine

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:264-33-5 SDS

264-33-5Upstream product

264-33-5Downstream Products

264-33-5Relevant academic research and scientific papers

Chemical Equivalent of Arene Monooxygenases: Dearomative Synthesis of Arene Oxides and Oxepines

Siddiqi, Zohaib,Wertjes, William C.,Sarlah, David

, p. 10125 - 10131 (2020)

Direct epoxidation of aromatic nuclei by cytochrome P450 monooxygenases is one of the major metabolic pathways of arenes in eukaryotes. The resulting arene oxides serve as versatile precursors to phenols, oxepines, or trans-dihydrodiol-based metabolites.

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