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3,4,4,5,5,6,6,7-Octahydro-1(3H),7-bi-2H-azepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34608-41-8

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34608-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34608-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,0 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34608-41:
(7*3)+(6*4)+(5*6)+(4*0)+(3*8)+(2*4)+(1*1)=108
108 % 10 = 8
So 34608-41-8 is a valid CAS Registry Number.

34608-41-8SDS

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 7-(azepane-1-yl)-3,4,5,6-tetrahydro-2H-azepine

1.2 Other means of identification

Product number -
Other names 3',4,4',5,5',6,6',7-octahydro-1(3H),7'-bi-2H-azepine

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:34608-41-8 SDS

34608-41-8Downstream Products

34608-41-8Relevant academic research and scientific papers

Copper-catalyzed aerobic oxidation of amines to imines under neat conditions with low catalyst loading

Patil, Rajendra D.,Adimurthy, Subbarayappa

supporting information; experimental part, p. 1695 - 1700 (2011/09/14)

The copper (I)-catalyzed direct synthesis of imines from amines under mild aerobic conditions is described. The method is applicable for the synthesis of various imines from corresponding amines such as benzylic, aliphatic, cyclic secondary, heteroaromatic species and the oxidative condensation of benzylamines with anilines extends the scope of the CuCl catalytic system. Noteworthy, solvent-free procedure, air as a benign oxidant, and the cheap and easy availability of the catalyst are the vital advantages of the method. Copyright

Aerobic oxidation of amines to imines catalyzed by bulk gold powder and by alumina-supported gold

Zhu, Bolin,Lazar, Mihaela,Trewyn, Brian G.,Angelici, Robert J.

experimental part, p. 1 - 6 (2009/02/08)

Both bulk gold powder (~50 μm particle size) and alumina-supported gold (50-150 nm) are highly active catalysts for the aerobic oxidative dehydrogenation of amines (CH-NH) to imines (C{double bond, long}N) under the mild conditions of 1 atm O2 and 100 °C. Reactions using the 5% Au/Al2O3 catalyst make efficient use of the gold metal and offer a practical synthesis of imines from amines. These studies add to the growing list of reactions that are catalyzed by bulk gold metal.

Non-nanogold catalyzed aerobic oxidation of secondary amines to imines

Zhu, Bolin,Angelici, Robert J.

, p. 2157 - 2159 (2008/02/08)

Bulk gold powder (~103 nm particle size) is a highly active catalyst for the oxidative dehydrogenation of secondary amines to imines under the mild conditions of 1 atm O2 and 60-100°C. The Royal Society of Chemistry.

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