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Ethanone, 1-[4-[(trimethylsilyl)oxy]-3-cyclohexen-1-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61692-28-2

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61692-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61692-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,9 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61692-28:
(7*6)+(6*1)+(5*6)+(4*9)+(3*2)+(2*2)+(1*8)=132
132 % 10 = 2
So 61692-28-2 is a valid CAS Registry Number.

61692-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-trimethylsilyloxycyclohex-3-en-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 4-acetyl-1-&lt

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:61692-28-2 SDS

61692-28-2Relevant academic research and scientific papers

1,3-Benzodithiolium Cation Mediated Cyclization Reactions

Rigby, James H.,Kotnis, Atul,Kramer, James

, p. 5078 - 5088 (1990)

General protocols for the construction of various ring systems employing cation olefin cyclizations initiated by the readily accessible 1,3-benzodithiolium ion are described.Several substituted tetralones and tetralins can be rapidly assembled by this methodology as can a variety of substituted bicyclooctane and tricyclic ring systems.The products of these transformations are amenable to interconversion into a range of functionalized species.

SYNTHESIS OF BICYCLOOCTANES BY A TANDEM DIELS-ALDER-CARBOCATION CYCLIZATION STRATEGY

Rigby, James H.,Kotnis, Atul S.

, p. 4943 - 4946 (2007/10/02)

The bicyclooctane ring system is assembled by a three-step process featuring a thermally induced cycloaddition followed by a 1,3-benzothiolium ion mediated cyclization onto an enol or silyl enol ether double bond.

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