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1-(8-Azidonaphthalen-1-yl)-1H-1,2,3-triazole-4-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91165-56-9

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91165-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91165-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,6 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91165-56:
(7*9)+(6*1)+(5*1)+(4*6)+(3*5)+(2*5)+(1*6)=129
129 % 10 = 9
So 91165-56-9 is a valid CAS Registry Number.

91165-56-9SDS

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 ethyl 1-(8-azido-1-naphthyl)-1H-1,2,3-triazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl-1-(8-azido-1-naphthyl)-1H-1,2,3-triazole-4-carboxylate

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:91165-56-9 SDS

91165-56-9Relevant academic research and scientific papers

Synthesis and Spectroscopic Studies of 1,1'-(1,8-Naphthylene)di-1H-1,2,3-triazoles

Nagawa, Yoshinobu,Honda, Koichi,Nakanishi, Hiroshi

, p. 2931 - 2936 (2007/10/02)

The first 1,8-diheteroaromatic naphthalenes, 1,1'-(1,8-naphthylene)di-1H-1,2,3-trizoles (1), were synthesized by 1,3-dipolar cycloadditions of 1,8-diazidonaphthalene to acetylenic esters.The spectral properties of these compounds were studied and compared with those of the corresponding 1-(1-naphthyl)-1H-1,2,3-triazoles (2).The two triazole rings at the peri-positions in 1 are in a face-to-face arrangement according to the results of 1H NMR spectra.The UV spectra of 1 are almost identical with each other and show a red shift from those of corresponding 2.No significant spectral differences between 1 and 2 were observed in the IR spectra.The fragment ion with two azirine groups at the peri-position in the naphthalene ring was observed in the MS spectra of 1.

Syntheses and Spectroscopic Studies of 1,8-Bistriazolylnaphthalenes

Honda, Koichi,Nakanishi, Hiroshi,Nagawa, Yoshinobu,Yabe, Akira

, p. 450 - 451 (2007/10/02)

The first 1,8-diheterocyclic naphthalenes, the 1,8-bis(1'H-1',2',3'-triazolyl)naphthalenes (1a - i), have been synthesized by 1,3-dipolar cycloadditions of 1,8-diazidonaphthalene to acetylenic esters or enolates of acetoacetic esters, and have strained structures as revealed by comparison of their spectral properties with those of the corresponding 1-(1'H-1',2',3'-triazolyl)naphthalenes.

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