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1,3-Oxazino[5,6:5,6]naphth[1,2-e][1,3]oxazine, 2,3,4,8,9,10-hexahydro-3,9-bis(phenylmethyl)is a complex organic compound characterized by a unique fused ring structure. It is a member of the oxazine class, which are heterocyclic compounds with a five-membered ring containing both oxygen and nitrogen atoms. This specific compound features a naphthalene ring fused with an oxazine ring, and it is further distinguished by the presence of two phenylmethyl groups attached at the 3 and 9 positions of the hexahydrooxazine ring. The distinctive structural attributes of 1,3-Oxazino[5,6:5,6]naphth[1,2-e][1,3]oxazine, 2,3,4,8,9,10-hexahydro-3,9-bis(phenylmethyl)- may endow it with special properties, suggesting potential applications in various fields such as medicinal chemistry and materials science.

58671-21-9

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58671-21-9 Usage

Uses

Used in Medicinal Chemistry:
1,3-Oxazino[5,6:5,6]naphth[1,2-e][1,3]oxazine, 2,3,4,8,9,10-hexahydro-3,9-bis(phenylmethyl)is used as a potential pharmaceutical agent for its unique structural features that may offer novel interactions with biological targets. Its heterocyclic nature and the presence of phenylmethyl groups could allow for specific binding affinities and activities against certain diseases or conditions.
Used in Materials Science:

Check Digit Verification of cas no

The CAS Registry Mumber 58671-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,7 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58671-21:
(7*5)+(6*8)+(5*6)+(4*7)+(3*1)+(2*2)+(1*1)=149
149 % 10 = 9
So 58671-21-9 is a valid CAS Registry Number.

58671-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,9-dibenzyl-2,4,8,10-tetrahydro-[1,3]benzoxazino[6,5-f][1,3]benzoxazine

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

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More Details:58671-21-9 SDS

58671-21-9Downstream Products

58671-21-9Relevant academic research and scientific papers

L-proline catalyzed unprecedented synthesis of novel naphtho-bis[1,3]oxazines under solvent-free conditions

Jadhav, Amol Maruti,Balwe, Sandip Gangadhar,Cho, Byung Gwon,Lim, Kwon Taek,Jeong, Yeon Tae

, p. 742 - 751 (2020)

An unprecedented l-proline-mediated one-pot sequential synthesis of novel 3,10-diphenyl-2,3,4,9,10,11-hexahydronaphtho[1,2-e:4,3-e′]bis[1,3]oxazine derivatives from 2,3-dihydroxynaphthalene, formaldehyde, and anilines under solvent-free conditions has been reported. Under the optimized reaction conditions, a broad range of substituted anilines and 2,3-dihydroxynaphthalene were found to participate in this transformation, thus affording new 3,10-diphenyl-2,3,4,9,10,11-hexahydronaphtho[1,2-e:4,3-e′]bis[1,3]oxaz-ines in good to excellent yields. This green procedure offers several advantages such as high atom economy, mild reaction conditions, short reaction time, easy workup and column chromatography-free method with a wide range of functional group tolerance.

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