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280-66-0

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280-66-0 Usage

General Description

2-Azabicyclo[3.3.1]nonane, also known as norbornane, is a bicyclic compound with a nitrogen atom in its ring structure. It is a colorless liquid with a unique molecular arrangement that gives it high stability and resistance to chemical reactions. This chemical is commonly used as a building block in organic synthesis, especially in the pharmaceutical industry. It is also used as a solvent and as a stabilizer in the production of polymers. Additionally, 2-Azabicyclo[3.3.1]nonane has potential applications in the field of materials science and as a precursor for the synthesis of various organic compounds. Overall, it is a versatile and important chemical with various industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 280-66-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 280-66:
(5*2)+(4*8)+(3*0)+(2*6)+(1*6)=60
60 % 10 = 0
So 280-66-0 is a valid CAS Registry Number.

280-66-0SDS

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 4-azabicyclo[3.3.1]nonane

1.2 Other means of identification

Product number -
Other names 2-Azabicyclo<3.3.1>nonan

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:280-66-0 SDS

280-66-0Downstream Products

280-66-0Relevant articles and documents

Synthesis of the diazatricyclic core of madangamines via cyclic N,O-acetalization-bridgehead reduction

Yoshimura, Yuta,Kusanagi, Takahiko,Kibayashi, Chihiro,Yamazaki, Naoki,Aoyagi, Sakae

experimental part, p. 1329 - 1354 (2009/04/11)

A new approach to synthesize the diazatricyclic core of the madangamine alkaloids is described. The synthesis involves intramolecular N,O-acetalization of the keto-aminophenol which enables rapid construction of the 2-azabicyclo[3.3.1]nonane skeleton. Red

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