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6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro- is a complex organic chemical compound with the molecular formula C11H9NO. It belongs to the class of indene derivatives, which are heterocyclic compounds containing a benzene ring fused to a pyrrolidine ring. This specific compound features an oxirene group (a three-membered ring with an oxygen atom) and a ketone functional group. It is a colorless solid and is used in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. The compound is also known for its potential applications in materials science and as a precursor in the preparation of other complex molecules.

6542-00-3

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6542-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6542-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6542-00:
(6*6)+(5*5)+(4*4)+(3*2)+(2*0)+(1*0)=83
83 % 10 = 3
So 6542-00-3 is a valid CAS Registry Number.

6542-00-3SDS

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 1a,6a-dihydro-1-oxacyclopropa[a]inden-6-one

1.2 Other means of identification

Product number -
Other names 2,3-epoxy-indan-1-one

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:6542-00-3 SDS

6542-00-3Upstream product

6542-00-3Downstream Products

6542-00-3Relevant academic research and scientific papers

Stereochemistry of the tetrabutylammonium cyanide-catalyzed cyanosylilation of cyclic α,β-epoxyketones - Dependence of the diastereoselectivity on the ring size

Aljarilla, Ana,Cordoba, Ruben,Csaky, Aurelio G.,Fernandez, Israel,Ortiz, Fernando Lopez,Plumet, Joaquin,Gomez, Gloria Ruiz

, p. 3969 - 3976 (2007/10/03)

The diastereoselective Bu4NCN-catalyzed addition of TMSCN to cyclic α,β-epoxyketones has been considered. Good diastereoselectivities were found, depending on the ring size of the starting material. Computational studies account for the observed diastereoselectivities. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Total synthesis of coriandrin and 7-demethylcoriandrin via a new synthesis of isocoumarins

Mal, Dipakranjan,Bandyopadhyay, Mousumi,Ghorai, Sujit K.,Datta, Kalyani

, p. 3677 - 3680 (2007/10/03)

Indenone epoxides 8, prepared from the corresponding indenones, have been shown to undergo clean thermal rearrangement to give isocoumarins 10 in high yields. This synthesis of isocoumarins, when applied to oxaindace-none 7, resulted in the total synthesis of coriandrin (1). (C) 2000 Elsevier Science Ltd.

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