N-butylpyridinium bromide

• CAS: 874-80-6
• Catalog Number: ACM874806
• Category: Pyridinium Ionic Liquids
• Molecular Weight: 171.67
• Molecular Formula: C9 H14 NBr
• Melting Point: 104-107°C
• Abbreviation: BpyBr
• Chemical Formula: [Bpy]Br
• MDL Number: MFCD00671496

Custom Q&A

What is the molecular formula of N-butylpyridinium bromide?

The molecular formula of N-butylpyridinium bromide is C9H14BrN.

What is the molecular weight of N-butylpyridinium bromide?

The molecular weight of N-butylpyridinium bromide is 216.12 g/mol.

When was N-butylpyridinium bromide first created?

N-butylpyridinium bromide was first created on July 19, 2005.

What is the IUPAC name of N-butylpyridinium bromide?

The IUPAC name of N-butylpyridinium bromide is 1-butylpyridin-1-ium bromide.

What are some synonyms for N-butylpyridinium bromide?

Some synonyms for N-butylpyridinium bromide are 1-Butylpyridinium bromide, 1-butylpyridin-1-ium bromide, and Butylpyridinium bromide.

What is the Canonical SMILES representation of N-butylpyridinium bromide?

The Canonical SMILES representation of N-butylpyridinium bromide is CCCC[N+]1=CC=CC=C1.[Br-].

How many hydrogen bond acceptor counts does N-butylpyridinium bromide have?

N-butylpyridinium bromide has 1 hydrogen bond acceptor count.

What is the topological polar surface area of N-butylpyridinium bromide?

The topological polar surface area of N-butylpyridinium bromide is 3.9 Ų.

How many covalently-bonded unit counts does N-butylpyridinium bromide have?

N-butylpyridinium bromide has 2 covalently-bonded unit counts.

Is the compound canonicalized?

Yes, the compound is canonicalized.

Synthetic Use

Upstream Synthesis Route 1

• 110-86-1
• 109-65-9

• 874-80-6

Reference: [1]Organic Process Research and Development,2018,vol. 22,p. 551 - 556

Downstream Synthesis Route 1

• 874-80-6
• 123-11-5

• 123-08-0
• 5736-88-9

Reference: [1] Letters in Organic Chemistry, 2011, vol. 8, # 1, p. 48 - 52

Downstream Synthesis Route 2

• 874-80-6

• 27361-14-4

Reference: [1]Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan,1935,vol. 55,p. 1313,1315
Chemische Berichte,1935,vol. 68,p. 2291,2293

Downstream Synthesis Route 3

• 874-80-6

• 53385-76-5

Reference: [1]Collection of Czechoslovak Chemical Communications,1974,vol. 39,p. 1210 - 1215

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