Structure

2,5-Dibromobenzenesulfonyl chloride

CAS
23886-64-8
Catalog Number
ACM23886648
Category
Bromine Series
Molecular Weight
334.41
Molecular Formula
C6H3Br2ClO2S

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What is the molecular formula of 2,5-Dibromobenzenesulfonyl chloride?

The molecular formula is C6H3Br2ClO2S.

What is the molecular weight of 2,5-Dibromobenzenesulfonyl chloride?

The molecular weight is 334.41 g/mol.

What is the IUPAC Name of 2,5-Dibromobenzenesulfonyl chloride?

The IUPAC Name is 2,5-dibromobenzenesulfonyl chloride.

What is the InChI of 2,5-Dibromobenzenesulfonyl chloride?

The InChI is InChI=1S/C6H3Br2ClO2S/c7-4-1-2-5(8)6(3-4)12(9,10)11/h1-3H.

What is the InChIKey of 2,5-Dibromobenzenesulfonyl chloride?

The InChIKey is ZLMPLIWURYRGEB-UHFFFAOYSA-N.

What is the Canonical SMILES of 2,5-Dibromobenzenesulfonyl chloride?

The Canonical SMILES is C1=CC(=C(C=C1Br)S(=O)(=O)Cl)Br.

What is the CAS number of 2,5-Dibromobenzenesulfonyl chloride?

The CAS number is 23886-64-8.

What is the European Community (EC) Number of 2,5-Dibromobenzenesulfonyl chloride?

The European Community (EC) Number is 623-873-5.

Is 2,5-Dibromobenzenesulfonyl chloride a covalently-bonded unit?

Yes, it is a covalently-bonded unit.

Upstream Synthesis Route 1

  • 106-37-6
  • 23886-64-8

Reference: [1]Huntress; Carten
[Journal of the American Chemical Society, 1940, vol. 62, p. 511,512]
[2]Nakamura, Tsuyoshi; Yonesu, Kiyoaki; Mizuno, Yumiko; Suzuki, Chie; Sakata, Yuki; Takuwa, Yoh; Nara, Futoshi; Satoh, Susumu
[Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 10, p. 3548 - 3564]
[3]Skhiri, Aymen; Salem, Ridha Ben; Soulé, Jean-Francois; Doucet, Henri
[Synthesis, 2016, vol. 48, # 18, p. 3097 - 3106]
[4]Current Patent Assignee: UNIVERSITY OF CALIFORNIA - US2018/209987, 2018, A1
Location in patent: Paragraph 0132; 0134

Downstream Synthesis Route 1

  • 23886-64-8
  • 38441-47-3

Reference: [1]Grillot et al.
[Journal of the American Chemical Society, 1954, vol. 76, p. 3969]

Downstream Synthesis Route 2

  • 23886-64-8
  • 7467-11-0

Reference: [1]Huntress; Carten
[Journal of the American Chemical Society, 1940, vol. 62, p. 511,512]
[2]Bahlmann
[Justus Liebigs Annalen der Chemie, 1876, vol. 181, p. 203]

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

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