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2H-Indeno[5,6-b]oxirene, octahydro- is a complex organic chemical compound with the molecular formula C11H14O. It is a derivative of indeno[5,6-b]oxirene, which is a type of oxirene, a cyclic ether with an epoxide group. The octahydro prefix indicates that the compound has undergone hydrogenation, resulting in the saturation of its carbon-carbon double bonds. This specific compound features a seven-membered ring with a fused six-membered ring, containing one oxygen atom in the form of an epoxide. It is an important intermediate in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity.

6784-63-0

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6784-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6784-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6784-63:
(6*6)+(5*7)+(4*8)+(3*4)+(2*6)+(1*3)=130
130 % 10 = 0
So 6784-63-0 is a valid CAS Registry Number.

6784-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-epoxy-cis-bicyclo<4.3.0>nonane

1.2 Other means of identification

Product number -
Other names (2aR,5aS)-Octahydro-1-oxa-cyclopropa[f]indene

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:6784-63-0 SDS

6784-63-0Relevant academic research and scientific papers

Liquid-phase synthesis of cyclic diene diepoxides using metal halides and hydrogen peroxide

Alimardanov, Kh. M.,Sadygov,Garibov,Abdullaeva, M. Ya.

, p. 1302 - 1308 (2013/02/21)

Optimal conditions were found for induced hydroxyhalogenation of cyclic dienes (tetrahydroindene, 4-vinylcyclohexene and 5-vinyl- and 5-cyclohexenylbicyclo[2.2.1]hept-2-enes) in the system [MHlg-HA or HHlg]-H 2O2 (or NaClO). Dehydrohalogenation of the chloro- and bromohydrins thus obtained with powdered potassium carbonate gave the corresponding diepoxy derivatives, and their hydrolysis led to mixtures of stereoisomeric tetrahydric alcohols. Pleiades Publishing, Ltd., 2012.

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