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2,3-dihydro-1H-3a,7a-methanoindene is a complex organic chemical compound with the molecular formula C11H12. It is a derivative of the indene family, characterized by a bicyclic structure with a saturated six-membered ring fused to a five-membered ring. The compound is named based on its structure, where the "2,3-dihydro" prefix indicates the presence of two hydrogen atoms added to the parent compound, and the "methano" prefix suggests the presence of a single carbon bridge connecting the two rings. 2,3-dihydro-1H-3a,7a-methanoindene is of interest in organic chemistry and may have potential applications in the synthesis of various pharmaceuticals and materials. However, it is important to note that the specific properties, reactivity, and uses of 2,3-dihydro-1H-3a,7a-methanoindene would require further investigation and characterization.

3463-81-8

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3463-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3463-81-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3463-81:
(6*3)+(5*4)+(4*6)+(3*3)+(2*8)+(1*1)=88
88 % 10 = 8
So 3463-81-8 is a valid CAS Registry Number.

3463-81-8SDS

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 2,3-dihydro-1H-3a,7a-methanoindene

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:3463-81-8 SDS

3463-81-8Downstream Products

3463-81-8Relevant academic research and scientific papers

Homoaromatic Delocalization in the Transition State for Norcaradiene Formation

Bertsch, Achim,Grimme, Wolfram,Reinhardt, Gerd,Rose, Hermann,Warner, Philip M.

, p. 5112 - 5117 (2007/10/02)

The kinetics for the extrusion of benzene from norcaradiene adducts 11 and 12 have been measured.The high 11/12 rate ratio, 8.9E3, was shown to be due to homoaromatic interactions in the cycloreversion transition state emanating from 11.This conclusion was reached after studying the benzene extrusion kinetics for several model compounds, including 20.The syntheses of the requisite compounds are fully described.

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