4-Bromophenylacetyl chloride

• CAS: 37859-24-8
• Catalog Number: ACM37859248
• Category: Aryl
• Molecular Weight: 233.49
• Molecular Formula: C₆H₂F₄
• Synonyms: 4-BROMOPHENYLACETIC ACID CHLORIDE;(4-BROMO-PHENYL)-ACETYL CHLORIDE;2-(4-bromophenyl)ethanoyl chloride
• Density: 1.589 g/cm³
• Appearance: chips
• Hazard Statements: H302-H410
• RIDADR: UN 3261 8 / PGII
• Symbol: GHS07

Custom Q&A

What is the IUPAC name of 4-Bromophenylacetyl chloride?

The IUPAC name of 4-Bromophenylacetyl chloride is 2-(4-bromophenyl)acetyl chloride.

What is the molecular formula of 4-Bromophenylacetyl chloride?

The molecular formula of 4-Bromophenylacetyl chloride is C8H6BrClO.

What is the CAS number of 4-Bromophenylacetyl chloride?

The CAS number of 4-Bromophenylacetyl chloride is 37859-24-8.

How much does 4-Bromophenylacetyl chloride weigh?

4-Bromophenylacetyl chloride has a molecular weight of 233.49 g/mol.

What is the InChI of 4-Bromophenylacetyl chloride?

The InChI of 4-Bromophenylacetyl chloride is InChI=1S/C8H6BrClO/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4H,5H2.

How many hydrogen bond donor counts does 4-Bromophenylacetyl chloride have?

4-Bromophenylacetyl chloride has 0 hydrogen bond donor counts.

What is the topological polar surface area of 4-Bromophenylacetyl chloride?

The topological polar surface area of 4-Bromophenylacetyl chloride is 17.1Ų.

How many rotatable bond counts does 4-Bromophenylacetyl chloride have?

4-Bromophenylacetyl chloride has 2 rotatable bond counts.

Is 4-Bromophenylacetyl chloride a canonicalized compound?

Yes, 4-Bromophenylacetyl chloride is a canonicalized compound.

What is the complexity of 4-Bromophenylacetyl chloride?

The complexity of 4-Bromophenylacetyl chloride is 141.

Synthetic Use

Upstream Synthesis Route 1

• 1878-68-8

• 37859-24-8

Reference: [1]Molecular Crystals and Liquid Crystals (1969-1991),1988,vol. 155,p. 113 - 128

Downstream Synthesis Route 1

• 67-56-1
• 37859-24-8

• 41841-16-1

Reference: [1] Journal of Organic Chemistry, 2007, vol. 72, # 15, p. 5920 - 5922
[2] Journal of Labelled Compounds and Radiopharmaceuticals, 1996, vol. 38, # 5, p. 425 - 433
[3] Patent: WO2009/24906, 2009, A1, . Location in patent: Page/Page column 12

Downstream Synthesis Route 2

• 37859-24-8
• 506-82-1

• 6186-22-7

Reference: [1] Archiv der Pharmazie, 1992, vol. 325, # 12, p. 751 - 760

Downstream Synthesis Route 3

• 37859-24-8
• 74-85-1

• 4133-35-1

Reference: [1] Patent: EP1199307, 2002, A1, . Location in patent: Page 12

Downstream Synthesis Route 4

• 37859-24-8

• 74860-13-2

Reference: [1]Panayotov
[Doklady Bolgarskoi Akademii Nauk, 1957, vol. 10, p. 137,139]
[2]Location in patent: experimental part
Gudaparthi, Vijayalakshmi; Bharathi; Panda, Jagadeesh
[Asian Journal of Chemistry, 2010, vol. 22, # 7, p. 5323 - 5330]
[3]Jung, Hui Jin; Nam, Eun Hye; Park, Jin Young; Ghosh, Prithwish; Kim, In Su
[Bioorganic and Medicinal Chemistry Letters, 2021, vol. 37]

Downstream Synthesis Route 5

• 37859-24-8
• 100-66-3

• 67205-73-6

Reference: [1]Tetrahedron Letters,2015,vol. 56,p. 1575 - 1580

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