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750638-97-2

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750638-97-2 Usage

General Description

2,4-Diiodo-3-hydroxypyridine is a chemical compound with the molecular formula C5H3I2NO. It is a derivative of pyridine and has two iodine atoms attached to the 2 and 4 positions of the pyridine ring, as well as a hydroxyl group at the 3 position. 2,4-Diiodo-3-hydroxypyridine is commonly used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is also known for its potential biological activities and has been studied for its anti-cancer and anti-inflammatory properties. Additionally, 2,4-Diiodo-3-hydroxypyridine has been investigated for its potential use in imaging agents for positron emission tomography (PET) scans.

Check Digit Verification of cas no

The CAS Registry Mumber 750638-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,0,6,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 750638-97:
(8*7)+(7*5)+(6*0)+(5*6)+(4*3)+(3*8)+(2*9)+(1*7)=182
182 % 10 = 2
So 750638-97-2 is a valid CAS Registry Number.

750638-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diiodopyridin-3-ol

1.2 Other means of identification

Product number -
Other names 3-Pyridinol,2,4-diiodo

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:750638-97-2 SDS

750638-97-2Upstream product

750638-97-2Downstream Products

750638-97-2Relevant articles and documents

Preparation of functionalized 3,4-pyridynes via 2-magnesiated diaryl sulfonates

Lin, Wenwei,Chen, Ling,Knochel, Paul

, p. 2787 - 2797 (2007/10/03)

The preparation of functionalized 3,4-pyridynes of type 1 as highly reactive intermediates has been achieved by the controlled elimination of readily generated 2-magnesiated diaryl sulfonates of type 2 obtained by a low temperature I/Mg- or Br/Mg-exchange starting from the corresponding halides of type 3. After trapping with furan, moderate to good yields of the desired functionalized cycloadducts of type 4 are obtained. The addition of a magnesium arylthiolate or magnesium phenylselenide to 3,4-pyridyne followed by quenching with an electrophile is also described.

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