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2-Naphthalenecarbonyl azide, also known as 2-(1-azidocarboxylate)naphthalene, is an organic compound with the chemical formula C11H7N3O2. It is a derivative of naphthalene, featuring a carbonyl group (C=O) at the 2-position and an azide group (-N3) attached to the carbonyl carbon. 2-Naphthalenecarbonyl azide is of interest in chemical research due to its potential applications in the synthesis of various organic compounds, particularly those involving the formation of carbon-nitrogen bonds. The azide group in 2-naphthalenecarbonyl azide can participate in a variety of chemical reactions, such as the Staudinger reaction, which can lead to the formation of amines or other nitrogen-containing compounds. Its reactivity and the ability to form stable intermediates make it a valuable building block in organic synthesis.

1208-11-3

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1208-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1208-11:
(6*1)+(5*2)+(4*0)+(3*8)+(2*1)+(1*1)=43
43 % 10 = 3
So 1208-11-3 is a valid CAS Registry Number.

1208-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name naphthalene-2-carbonyl azide

1.2 Other means of identification

Product number -
Other names [2]naphthoyl azide

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1208-11-3 SDS

1208-11-3Relevant academic research and scientific papers

Synthesis of Acyl Azides from 1,3-Diketones via Oxidative Cleavage of Two C-C Bonds

Yu, Tian-Yang,Zheng, Zhao-Jing,Dang, Tong-Tong,Zhang, Fang-Xia,Wei, Hao

, p. 10589 - 10594 (2018/09/06)

A metal-free PhI(OAc)2-mediated method for the synthesis of acyl azides through oxidative cleavage of 1,3-diketones is described. This method is shown to have a broad substrate scope, providing a useful tool for multiproduct synthesis in a single procedure. A possible reaction pathway is proposed based on mechanistic studies.

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