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15366-65-1

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15366-65-1 Usage

General Description

5-Iodonicotinic acid is a chemical compound with the molecular formula C6H4INO2. It is a derivative of nicotinic acid and contains an iodine atom positioned at the 5th position of the pyridine ring. 5-IODONICOTINIC ACID is often used in organic synthesis and pharmaceutical research due to its potential as a building block in the production of various compounds. It is also used as a precursor in the synthesis of pharmaceutical drugs and agrochemicals. Additionally, 5-Iodonicotinic acid has been studied for its potential therapeutic properties, particularly in the treatment of various diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 15366-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15366-65:
(7*1)+(6*5)+(5*3)+(4*6)+(3*6)+(2*6)+(1*5)=111
111 % 10 = 1
So 15366-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4INO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,(H,9,10)

15366-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Iodonicotinic acid

1.2 Other means of identification

Product number -
Other names 5-iodopyridine-3-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:15366-65-1 SDS

15366-65-1Relevant articles and documents

A unified synthetic strategy for the indolopyridine alkaloid group

Lavilla, Rodolfo,Gullón, Francisco,Bosch, Joan

, p. 373 - 378 (2007/10/03)

Thermal or acetyl chloride induced cyclization of bromoenamide 10 affords the pentacyclic derivative 12 with high yield and regioselectivity. From this common synthetic intermediate, palladium-catalyzed reactions allow the total synthesis of indolopyridin

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