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14233-73-9

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14233-73-9 Usage

General Description

3-(2-hydroxy-1-naphthyl)propanenitrile is a chemical compound with the molecular formula C17H13NO. It is a nitrile derivative of 1-naphthol, with a hydroxy group attached to the 2-position of the naphthyl ring. The compound is a white to pale yellow solid and is used as a building block in organic synthesis, particularly in the synthesis of pharmaceuticals and other organic compounds. It has potential applications in the preparation of various functional materials and organic compounds due to its unique structure and reactivity. Additionally, the compound may also have potential biological activities, making it a subject of interest in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 14233-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,3 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14233-73:
(7*1)+(6*4)+(5*2)+(4*3)+(3*3)+(2*7)+(1*3)=79
79 % 10 = 9
So 14233-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H11NO/c14-9-3-6-12-11-5-2-1-4-10(11)7-8-13(12)15/h1-2,4-5,7-8,15H,3,6H2

14233-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-hydroxynaphthalen-1-yl)propanenitrile

1.2 Other means of identification

Product number -
Other names 3-(2-hydroxynaphthyl)propanenitrile

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:14233-73-9 SDS

14233-73-9Relevant articles and documents

Photoadditions of 1- and 2-Naphthols and Derivatives to Acrylonitrile. Conversion of the Cyclobutane Adducts to Cyanoethylnaphthols

Akhtar, Ikbal A.,McCullough, John J.

, p. 1447 - 1450 (1981)

The photoreactions of 1- and 2-naphthol, their trimethylsilyl (Me3Si) ethers, and 1-methoxynaphthalene with acrylonitrile in a 1:1 isopropyl alcohol-tert-butyl alcohol mixture have been investigated.Irradiation of 2-naphthol and acrylonitrile gives 7-cyano-2,3-benzobicycloocta-2,4-dien-6-ol (3) while 2-naphthol trimethylsilyl ether gives the trimethylsilyl ether of 3.Base treatment of 3 or 3 trimethylsilyl ether gave 1-(2-cyanoethyl)-2-naphthol.Photoaddition of 1-naphthol trimehylsilyl ether and acrylonitrile gives8-cyano-2,3-benzobicycloocta-2,4-dien-1-ol trimethylsilyl ether, which is converted to the parent alcohol (6) by acid or to 2-(2-cyanoethyl)-1-naphthol (7) by base.The latter was also isolated in poor yield from the photolysis of 1-naphthol and acrylonitrile.Photoaddition of 1-methoxynaphthalene and acrylonitrile affords 1-methoxy-8-cyano-2,3-benzobicycloocta-2,4-diene (8) and endo-4-methoxy-7-cyano-2,3-benzobicycloocta-2,4-diene (9), in the ratio 1:1. 2,6-Dimethoxynaphthalene adds to acrylonitrile, giving the 7-cyano-6-methoxy-2,3-(2'-methoxy)benzobicycloocta-2,4-diene (16).These photoadditions are of possible synthetic utility for the ortho cyanoethylation of phenols.

Synthesis of musafluorone: A naphthoxanthenone isolated from Musa acuminata

Duque, Luisa,Restrepo, Catalina,Sáez, Jairo,Gil, Jesús,Schneider, Bernd,Otálvaro, Felipe

scheme or table, p. 4640 - 4643 (2010/09/10)

5-Methoxy-3H-naphtho[2,1,8-mna]xanthen-3-one (musafluorone, 1), the only naphthoxanthenone reported so far from Musaceae, was synthesized starting from 2-naphthol in nine steps and resulted in an overall yield of 3%. Grignard addition of phenylmagnesium b

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