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909036-46-0 Usage


2-Chloro-3-iodo-4-pyridinamine can be used as a useful synthetic intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 909036-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,0,3 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 909036-46:
170 % 10 = 0
So 909036-46-0 is a valid CAS Registry Number.

909036-46-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H33136)  4-Amino-2-chloro-3-iodopyridine, 95%   

  • 909036-46-0

  • 250mg

  • 767.0CNY

  • Detail
  • Alfa Aesar

  • (H33136)  4-Amino-2-chloro-3-iodopyridine, 95%   

  • 909036-46-0

  • 1g

  • 2129.0CNY

  • Detail
  • Aldrich

  • (ADE000415)  2-Chloro-3-iodopyridin-4-amine  AldrichCPR

  • 909036-46-0

  • ADE000415-1G

  • 4,512.69CNY

  • Detail



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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017


1.1 GHS Product identifier


1.2 Other means of identification

Product number -
Other names 2-chloro-3-iodo-4-pyridylamine

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:909036-46-0 SDS

909036-46-0Upstream product

909036-46-0Relevant articles and documents

Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols

Balfour, Michael N.,Franco, Caio H.,Moraes, Carolina B.,Freitas-Junior, Lucio H.,Stefani, Hélio A.

, p. 202 - 212 (2017)

A library of 16 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols 17–32 has been synthesized for use in biological testing against Trypanosoma cruzi, the protozoan parasite that causes Chagas disease. The 4-substituted 2-(1H-pyrrolo[3,2-c]pyridi

Organic compound, electroluminescent device containing organic compound and applications of electroluminescent device


Paragraph 0115-0117, (2020/06/17)

The invention discloses an organic compound with a structure represented by a formula (I), wherein the LUMO energy level of the compound is reduced by linking an aza aromatic ring structure (a structure represented by a formula (II)), so that the electronic conductivity of the material is improved, and the compound is suitable for being used as an electronic material (such as an electron transportmaterial, an electron injection material, a hole blocking material and the like). According to the invention, the organic compound as an electron type material, particularly an electron transmissionmaterial, can be matched with hole type materials (such as a hole transmission material, a hole injection material and an electron blocking material), so that the transmission of electrons and holes is balanced, and the service life of a device is prolonged.



Page/Page column 171-172, (2017/01/09)

Disclosed are compounds of Formula (I) or salts thereof, wherein HET is a heteroaryl selected from pyrrolo[2,3 b]pyridinyl, pyrrolo[2,3 d]pyrimidinyl, pyrazolo[3,4 b]pyridinyl, pyrazolo[3,4 d]pyrimidinyl, imidazolo[4,5 b]pyridinyl, and imidazolo[4,5 d]pyrimidinyl, wherein said heteroaryl is attached to the pyridinyl group in the compound of Formula (I) by a nitrogen ring atom in said heteroaryl and wherein said heteroaryl is substituted with zero to 2 Rb; A is pyrazolyl, imidazolyl, triazolyl, isoxazolyl, oxadiazolyl or dihydroisoxazolyl, each substituted with zero or 1 Ra; and R3, Ra, and Rb are define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases, or in the treatment of cancer.

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