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1,8-diazabicyclo[6.4.3]pentadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84905-03-3

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84905-03-3 Usage

Chemical structure

Bicyclic with a strong base character

Usage

Catalyst in organic reactions

Applications

Synthesis of pharmaceuticals, agrochemicals, and polymers

Bond formation

Promotes carbon-carbon and carbon-nitrogen bonds

Reactivity

High

Popularity

Widely used by researchers and industrial chemists

Hazard

Can be hazardous if not handled and stored properly

Safety precautions

Use in a well-ventilated environment

Check Digit Verification of cas no

The CAS Registry Mumber 84905-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,0 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84905-03:
(7*8)+(6*4)+(5*9)+(4*0)+(3*5)+(2*0)+(1*3)=143
143 % 10 = 3
So 84905-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H26N2/c1-2-4-9-15-11-6-5-10-14(8-3-1)12-7-13-15/h1-13H2

84905-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-diazabicyclo[6.4.3]pentadecane

1.2 Other means of identification

Product number -
Other names 1,6-Diazabicyclo<6.4.3>pentadecane

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:84905-03-3 SDS

84905-03-3Downstream Products

84905-03-3Relevant academic research and scientific papers

SYNTHESIS OF MEDIUM-RING BICYCLIC BRIDGEHEAD DIAMINES FROM MONOCYCLIC DIAMINES VIA α-AMINOAMMONIUM IONS

Alder, Roger W.,Eastment, Paul,Moss, Richard E.,Sessions, Richard B.,Stringfellow, Martin A.

, p. 4181 - 4184 (2007/10/02)

Condensation of 4-chlorobutanal and 5-chloropentanal with six cyclic diamines gave twelve α-aminoammonium salts; cleavage of these with LiAlH4 gave medium-ring bicyclic diamines.

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