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2-Chloro-5-iodo-4-pyridinamine

Detailed Information

  • Product Name:2-Chloro-5-iodo-4-pyridinamine
  • CasNo.:800402-12-4
  • MF:C5H4ClIN2
  • MW:254.458

pd_nature

  • Purity:99%
  • pd_boiling:126-127°
  • Packing:
  • Throughput:

Product Details;

CasNo: 800402-12-4

MF: C5H4ClIN2

Buy Good Quality 2-Chloro-5-iodo-4-pyridinamine 800402-12-4 with a minimum purity of 99%

  • Molecular Formula:C5H4ClIN2
  • Molecular Weight:254.458
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:126-127° 
  • Boiling Point:367.751oC at 760 mmHg 
  • PKA:2.96±0.42(Predicted) 
  • Flash Point:176.21oC 
  • PSA:38.91000 
  • Density:2.139g/cm3 
  • LogP:2.50300 

2-Chloro-5-iodo-4-pyridinamine(Cas 800402-12-4) Usage

General Description

2-Chloro-5-iodo-4-pyridinamine is a chemical compound that has the molecular formula C5H3ClIN3. It is a derivative of pyridine and contains both chlorine and iodine atoms. 2-Chloro-5-iodo-4-pyridinamine is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. It has also found applications in the field of medicinal and agrochemical research. The presence of halogen substituents in its structure makes it a valuable building block for the development of new chemical entities with potential biological activities. Additionally, 2-Chloro-5-iodo-4-pyridinamine is known for its reactivity and can undergo various chemical transformations under suitable reaction conditions.

InChI:InChI=1/C5H4ClIN2/c6-5-1-4(8)3(7)2-9-5/h1-2H,(H2,8,9)

800402-12-4 Relevant articles

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

-

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

The invention discloses an organic compo...

PYRIMIDINE OR PYRIDOPYRIDONE COMPOUND AND APPLICATION THEREOF

-

Paragraph 0046; 0069, (2018/11/21)

The present invention discloses a pyrimi...

Synthesis, molecular docking, antimycobacterial and antimicrobial evaluation of new pyrrolo[3,2-c]pyridine Mannich bases

Jose, Gilish,Suresha Kumara, Tholappanavara H.,Sowmya, Haliwana B.V.,Sriram, Dharmarajan,Guru Row, Tayur N.,Hosamani, Amar A.,More, Sunil S.,Janardhan, Bhavya,Harish,Telkar, Sandeep,Ravikumar, Yalegara Siddappa

, p. 275 - 288 (2017/03/24)

In this report, we describe the synthesi...

HETEROARYL SUBSTITUTED AMINOPYRIDINE COMPOUNDS

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

Disclosed are compounds of Formula (I) o...

800402-12-4 Process route

4-Amino-2-chloropyridine
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4-Amino-2-chloropyridine

2-chloro-4-amino-5-iodopyridine
800402-12-4

2-chloro-4-amino-5-iodopyridine

2-chloro-3-iodo-pyridin-4-ylamine
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2-chloro-3-iodo-pyridin-4-ylamine

2-chloro-3,5-diiodopyridin-4-amine
1171919-00-8

2-chloro-3,5-diiodopyridin-4-amine

Conditions
Conditions Yield
With potassium acetate; Iodine monochloride; In acetic acid; at 70 ℃; for 4h; Inert atmosphere;
49.7%
With potassium acetate; Iodine monochloride; acetic acid; at 70 ℃; for 4h; Inert atmosphere;
49.7%
With potassium acetate; Iodine monochloride; at 45 ℃; for 96h; pH=5.5; Inert atmosphere; aq. buffer;
45%
30%
11%
With potassium acetate; Iodine monochloride; acetic acid; at 70 ℃; for 4h; Inert atmosphere;
4-Amino-2-chloropyridine
14432-12-3

4-Amino-2-chloropyridine

2-chloro-4-amino-5-iodopyridine
800402-12-4

2-chloro-4-amino-5-iodopyridine

2-chloro-3,5-diiodopyridin-4-amine
1171919-00-8

2-chloro-3,5-diiodopyridin-4-amine

Conditions
Conditions Yield
With sodium acetate; Iodine monochloride; acetic acid; at 60 ℃; for 2h;
45%
50%

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