Bromoacetyl chloride

• CAS: 22118-09-8
• Catalog Number: ACM22118098
• Category: Bromine Series
• Molecular Weight: 157.39
• Molecular Formula: C₂H₂BrClO
• Synonyms: BROMOACETYL CHLORIDE;Acetyl chloride, bromo-;BROMOACETYL CHLORIDE, (CONTAINS VARYING AMOUNTS OF CHLOROACETYL CHLORIDE): 65%;monobromo acetyl chloride;Bromoacetic acid chloride;2-bromoethanoyl chloride
• Density: 1.89

Custom Q&A

What is the PubChem CID of Bromoacetyl chloride?

PubChem CID 89602

What is the molecular formula of Bromoacetyl chloride?

C2H2BrClO

What is the molecular weight of Bromoacetyl chloride?

157.39 g/mol

What is the IUPAC name of Bromoacetyl chloride?

2-bromoacetyl chloride

What is the InChI of Bromoacetyl chloride?

InChI=1S/C2H2BrClO/c3-1-2(4)5/h1H2

What is the InChIKey of Bromoacetyl chloride?

SYZRZLUNWVNNNV-UHFFFAOYSA-N

What is the canonical SMILES of Bromoacetyl chloride?

C(C(=O)Cl)Br

What is the CAS number of Bromoacetyl chloride?

22118-09-8

What is the European Community (EC) number of Bromoacetyl chloride?

244-790-7

Is Bromoacetyl chloride a covalently-bonded unit?

Yes

Synthetic Use

Downstream Synthesis Route 1

• 110-89-4
• 22118-09-8

• 1796-25-4
• 1440-60-4

Reference: [1] Chemistry of Natural Compounds, 2013, vol. 48, # 6, p. 1047 - 1053[2] Khim. Prir. Soedin., 2012, vol. 48, # 6, p. 924 - 929,6

Downstream Synthesis Route 2

• 110-91-8
• 22118-09-8

• 1440-61-5

Reference: [1] Chemistry of Natural Compounds, 2013, vol. 48, # 6, p. 1047 - 1053[2] Khim. Prir. Soedin., 2012, vol. 48, # 6, p. 924 - 929,6

Downstream Synthesis Route 3

• 67-56-1
• 22118-09-8

• 96-32-2

Reference: [1] Journal of Molecular Structure, 1991, vol. 246, # 3/4, p. 267 - 278

Downstream Synthesis Route 4

• 110-91-8
• 22118-09-8

• 40299-87-4

Reference: [1]Kushner et al.
[Journal of Organic Chemistry, 1951, vol. 16, p. 1283,1287]
[2]Ronsisvalle; Marrazzo; Prezzavento; Pasquinucci; Vittorio; Pittala; Pappalardo; Cacciaguerra; Spampinato
[Journal of medicinal chemistry, 1998, vol. 41, # 10, p. 1574 - 1580]
[3]Location in patent: experimental part
Zhang, Xian; He, Yantao; Liu, Sijiu; Yu, Zhihong; Jiang, Zhong-Xing; Yang, Zhenyun; Dong, Yuanshu; Nabinger, Sarah C.; Wu, Li; Gunawan, Andrea M.; Wang, Lina; Chan, Rebecca J.; Zhang, Zhong-Yin
[Journal of Medicinal Chemistry, 2010, vol. 53, # 6, p. 2482 - 2493]
[4]Location in patent: scheme or table
Zhou, Bo; He, Yantao; Zhang, Xian; Xu, Jie; Luo, Yong; Wang, Yuehong; Franzblau, Scott G.; Yang, Zhenyun; Chan, Rebecca J.; Liu, Yan; Zheng, Jianyu; Zhang, Zhong-Yin
[Proceedings of the National Academy of Sciences of the United States of America, 2010, vol. 107, # 10, p. 4573 - 4578]
[5]Pissinate, Kenia; Villela, Anne Drumond; Rodrigues, Valnês; Giacobbo, Bruno Couto; Grams, Estêvão Silveira; Abbadi, Bruno Lopes; Trindade, Rogério Valim; Roesler Nery, Laura; Bonan, Carla Denise; Back, Davi Fernando; Campos, Maria Martha; Basso, Luiz Augusto; Santos, Diógenes Santiago; Machado, Pablo
[ACS Medicinal Chemistry Letters, 2016, vol. 7, # 3, p. 235 - 239]

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