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67388-67-4

Bicyclo[3.3.1]nonan-2-one, 6-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67388-67-4

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67388-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67388-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,8 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67388-67:
(7*6)+(6*7)+(5*3)+(4*8)+(3*8)+(2*6)+(1*7)=174
174 % 10 = 4
So 67388-67-4 is a valid CAS Registry Number.

67388-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name endo-6-Hydroxy-bicyclo[3,3,1]nonan-2-on

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:67388-67-4 SDS

67388-67-4Downstream Products

67388-67-4Relevant articles and documents

SYNTHESIS OF 1-HYDROXY-2-(N-SUBSTITUTED)AZATWISTANES

Kadzyauskas, P. P.,Malinauskene, Yu. A.,Butkus, E. P.,Zefirov, N. S.

, p. 727 - 729 (1980)

The reductive amination of bicyclononane-2,6-dione with benzylamine or isopropylamine in the presence of sodium borohydride proceeds with the formation of 1-hydroxy-2-(N-substituted)azatwistanes.When 1-hydroxy-2-benzyl-2-azatwistane is refluxed with acetic anhydride, the ring is opened to give 2-acetoxy-6-acetylbenzylaminobicyclononane.The structures of the synthesized compounds were proved by means of the IR and PMR spectra and the results of elementary analysis.

Synthesis and chiroptical properties of enantiopure tricyclo[4.3.0.03,8]nonane-4,5-dione (twistbrendanedione)

Butkus, Eugenius,Dilinskas, Albinas,Stoncius, Sigitas,Rozenbergas, Ricardas,Urbanova, Marie,Setnicka, Vladimir,Bour, Petr,Volka, Karel

, p. 633 - 638 (2007/10/03)

The synthesis of chiral tricyclo[4.3.0.03,8]nonane-4,5-dione was accomplished starting from enantiomerically pure (+)-(1S,5S)-bicyclo[3.3.1]nonane-2,6-dione 1. Ring contraction of the latter with thallium(III) nitrate proceeded with high stereo

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