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4,5-Didehydro-4H-benzo[b]quinolizine-5-ium is a complex organic compound with the molecular formula C13H9N. It is a derivative of benzoquinolizine, a fused-ring system consisting of a benzene ring and a quinazoline ring. This particular compound is characterized by the presence of a double bond between the 4 and 5 positions, which results in the loss of two hydrogen atoms. The compound exhibits a positively charged nitrogen atom, indicating its quaternary nature. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its stability, solubility, and potential applications, make it a subject of interest in organic chemistry research.

260-62-8

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260-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 260-62-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 260-62:
(5*2)+(4*6)+(3*0)+(2*6)+(1*2)=48
48 % 10 = 8
So 260-62-8 is a valid CAS Registry Number.

260-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name acridizinium

1.2 Other means of identification

Product number -
Other names Acridizinium

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:260-62-8 SDS

260-62-8Downstream Products

260-62-8Relevant academic research and scientific papers

Gas-phase arylmethyl transfer and cyclodeamination of argentinated N-arylmethyl-pyridin-2-ylmethanimine

Sun, Hezhi,Wang, Lin,Pan, Yuanjiang

, p. 169 - 175 (2014)

In collisional activation of argentinated N-arylmethyl-pyridin-2- ylmethanimine, a neutral molecule of AgNH2 is eliminated, carrying one hydrogen from the methylene and the other one from the ortho position (relative to the ipso carbon) of the aryl ring. Taking argentinated N-benzyl-pyridin-2-ylmethanimine for example, the proposition that the AgNH 2 loss results from intramolecular arylmethyl transfer combined with cyclodeamination is rationalized by deuterium labeling experiments, blocking experiments, and theoretical calculations. The structure of the final product ion from loss of AgNH2 was confirmed further by multistage mass spectrometry. [Figure not available: see fulltext.]

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