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5,6,8,9-Tetrahydro-5,8-methano-7H-benzocyclohepten-7-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22099-65-6

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22099-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22099-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22099-65:
(7*2)+(6*2)+(5*0)+(4*9)+(3*9)+(2*6)+(1*5)=106
106 % 10 = 6
So 22099-65-6 is a valid CAS Registry Number.

22099-65-6SDS

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 3.4-Benzo-bicyclo[3.2.1]octenon-(7)

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:22099-65-6 SDS

22099-65-6Relevant academic research and scientific papers

Norcaradienes from the intramolecular cyclopropanation reactions of diazomethyl ketones. Valuable intermediates for the synthesis of polycyclic diterpenes

Morris, Jonathan C.,Mander, Lewis N.,Hockless, David C. R.

, p. 455 - 467 (2007/10/03)

The intramolecular cyclopropanation reactions of the aromatic ring in tetrahydronaphthyl diazomethyl ketones initiated by rhodium(II) and copper(II) derived transition metal catalysts afford stable norcaradiene products. Further elaboration has led to pentacyclic structures that have considerable potential for the expeditious synthesis of complex polycyclic diterpenes.

Rearrangement of Bicyclooct-2-en-6-yl and Benzobicyclooctenyl Cations

Kirmse, Wolfgang,Moench, Dietmar

, p. 1287 - 1294 (2007/10/02)

The ketones 9, 27, and 51 were prepared by modified or novel routes.The analogous tosylhydrazones 10, 28, and 52 were photolyzed in 0.5 N NaOH to generate the carbocations 15, 34, and 53, respectively, by way of diazonium precursors. 2,3-Unsaturati

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