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113423-89-5

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113423-89-5 Usage

Explanation

Different sources of media describe the Explanation of 113423-89-5 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 15 carbon (C), 10 hydrogen (H), 4 nitrogen (N), and 2 oxygen (O) atoms.
2. The compound is derived from the 1,2,3-triazole ring system, which is a five-membered ring containing three nitrogen atoms.
3. The compound features a naphthalene group, which is a fused pair of benzene rings. This group is known for its aromatic properties and is commonly found in various organic compounds.
4. Due to its unique structure and functional groups, the compound has potential uses in various fields, including the development of new pharmaceuticals, materials with specific properties, and as a building block for organic synthesis.
5. The molecule contains a carboxylic acid group (-COOH), which is a functional group consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom.
6. The presence of the carboxylic acid group allows for further functionalization and modification of the molecule through various chemical reactions, such as esterification, amide formation, and other condensation reactions. This enables the creation of a wide range of derivatives with different properties and potential applications.
7. The compound has an aromatic structure due to the presence of the naphthalene and 1,2,3-triazole groups. Additionally, it is a heterocyclic compound, as it contains rings with both carbon and heteroatoms (nitrogen and oxygen).

Derivative of 1,2,3-triazole

Yes

Contains a naphthalene group

Yes

Potential applications

Medicinal chemistry, materials science, and organic synthesis

Carboxylic acid group

Present

Suitability for functionalization and modification

High

Structure

Aromatic and heterocyclic

Check Digit Verification of cas no

The CAS Registry Mumber 113423-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,2 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113423-89:
(8*1)+(7*1)+(6*3)+(5*4)+(4*2)+(3*3)+(2*8)+(1*9)=95
95 % 10 = 5
So 113423-89-5 is a valid CAS Registry Number.

113423-89-5SDS

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 1-naphthalen-1-yltriazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-(naphthalen-1-yl)-1H-1,2,3-triazole-4-carboxylic acid

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:113423-89-5 SDS

113423-89-5Relevant articles and documents

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 (1987)

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.

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