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Decahydro-2H,5aH-4a,9a-epoxydibenzo[b,f]oxepin-5a-ol is a complex organic compound with the molecular formula C14H16O3. It is a derivative of dibenzo[b,f]oxepin, a type of cyclic compound consisting of two benzene rings fused to an oxepane ring. The compound features a unique structure with a hydroxyl group (-OH) at the 5a position, an epoxy bridge between the 4a and 9a positions, and ten hydrogen atoms in its decahydro form. This chemical is known for its potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various bioactive compounds. Its specific properties, such as solubility, reactivity, and stability, can be influenced by the presence of the epoxy and hydroxyl functional groups, making it a subject of interest for further exploration in the field of organic chemistry.

1489-92-5

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1489-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1489-92-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1489-92:
(6*1)+(5*4)+(4*8)+(3*9)+(2*9)+(1*2)=105
105 % 10 = 5
So 1489-92-5 is a valid CAS Registry Number.

1489-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name decahydro-2h,5ah-4a,9a-epoxydibenzo[b,f]oxepin-5a-ol

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:1489-92-5 SDS

1489-92-5Downstream Products

1489-92-5Relevant academic research and scientific papers

New directions in the condensation reactions of cyclohexanone and its Mannich base

Fedotova,Kapitonova,Reshetov,Tsimbalenko

, p. 773 - 777 (1997)

An unusual direction was found in the condensation of cyclohexanone and its Mannich base, leading to the formation of previously unknown polycydic spirohydrochromans. The structure of the compounds was confirmed by 13C NMR and mass spectrometry. 1998 Plenum Publishing Corporation.

Alkylation of manganese(II) tetraphenylporphyrin by a synthetic antimalarial trioxane

Berrien, Jean-Francois,Provot, Olivier,Myarargue, Joelle,Coquillay, Michel,Ciceron, Liliane,Gay, Frederick,Danis, Martin,Robert, Anne,Meunier, Bernard

, p. 2859 - 2864 (2003)

The synthesis and the antimalarial activity of a new kind of polycyclic 1,2,4-trioxanes are reported. The alkylation of the heme model MnIITPP by the biologically active (IC 50 = 320 nmol L-1) hemiperketal 2 is presented.

Properties and antiphage activity of condensed hydro(thio)chromans and their copper complexes

Fedotova,Lipatova,Kapitonova,Reshetov,Plotnikov,Kharchenko

, p. 1131 - 1135 (1996)

Research into the reactivity of carbonyl-substituted spirohydrochromans with hydrogen sulfide under the influence of protic and aprotic acids was continued for the case of 3,4,5,6,7,8-hexahydrospiro[chromene-2,1′-cyclohexan]-2-one. The general nature of the reactions was established. Complexes of copper(II) with substituted hydro(thio)chromans were obtained. The results from investigation of the antiphage activity of the synthesized compounds are presented. 1997 Plenum Publishing Corporation.

CONDENSATIONS OF ALDEHYDES AND KETONES. XXV. CONDENSATION PRODUCTS OF 2-DIMETHYLAMINOMETHYLCYCLOHEXANONE WITH CYCLOPENTANONE

Akimova, T. I.,Kosenko, S. V.,Tilichenko, M. N.

, p. 2271 - 2277 (2007/10/02)

In the condensation of 2-dimethylaminomethylcyclohexanane with cyclopentanone, in addition to (2-oxocyclohexyl)(2-oxocyclopentyl)-methane, by-products are also formed, namely, 2', 8a-epoxy-4a,5,6,7,8,8a-hexahydrochromane-2-spiro-2'-hydroxycyclohexane and

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