3,5-Diiodopyridin-4-amine

• CAS: 98136-86-8
• Catalog Number: ACM98136868
• Category: Pyridines
• Molecular Weight: 345.91
• Molecular Formula: C5H4I2N2
• Synonyms: 4-Amino-3,5-diiodopyridine

Custom Q&A

What is the molecular formula of 3,5-Diiodopyridin-4-amine?

The molecular formula is C5H4I2N2.

When was the structure of 3,5-Diiodopyridin-4-amine created and last modified?

The structure was created on 2009-05-30 and last modified on 2023-12-30.

What is the IUPAC name of 3,5-Diiodopyridin-4-amine?

The IUPAC name is 3,5-diiodopyridin-4-amine.

What is the InChI of 3,5-Diiodopyridin-4-amine?

The InChI is InChI=1S/C5H4I2N2/c6-3-1-9-2-4(7)5(3)8/h1-2H,(H2,8,9).

What is the molecular weight of 3,5-Diiodopyridin-4-amine?

The molecular weight is 345.91 g/mol.

How many hydrogen bond donor counts are there in 3,5-Diiodopyridin-4-amine?

There is 1 hydrogen bond donor count.

What is the exact mass of 3,5-Diiodopyridin-4-amine?

The exact mass is 345.84639 g/mol.

How many heavy atoms are there in 3,5-Diiodopyridin-4-amine?

There are 9 heavy atoms.

Is 3,5-Diiodopyridin-4-amine considered as canonicalized compound?

Yes, the compound is canonicalized.

What is the topological polar surface area of 3,5-Diiodopyridin-4-amine?

The topological polar surface area is 38.9 Å2.

Synthetic Use

Upstream Synthesis Route 1

• 504-24-5

• 88511-27-7
• 98136-86-8

Reference: [1] Journal of Organic Chemistry, 2012, vol. 77, # 11, p. 5006 - 5016

Upstream Synthesis Route 2

• 504-24-5

• 98136-86-8

Reference: [1] Patent: CN104262242, 2016, B, . Location in patent: Paragraph 0030; 0031

Upstream Synthesis Route 3

• 504-24-5

• 88511-27-7
• 98136-86-8

Reference: [1]Journal of Organic Chemistry,2012,vol. 77,p. 5006 - 5016
[2]Organic Process Research and Development,2018,vol. 22,p. 1276 - 1281
[3]Patent: WO2005/105814,2005,A1 .Location in patent: Page/Page column 96
[4]Patent: US2064945,1931,
[5]Patent: US2064945,1931,

Downstream Synthesis Route 1

• 98136-86-8
• 74-88-4

• 119038-43-6

Reference: [1]Journal fur praktische Chemie (Leipzig 1954),1959,vol. <4> 8,p. 156,165

* For details of the synthesis route, please refer to the original source to ensure accuracy.