5-Bromo-2-iodobenzotrifluoride

• CAS: 364-12-5
• Catalog Number: ACM364125
• Category: Bromine Series
• Molecular Weight: 350.90
• Molecular Formula: C₇H₃BrF₃I

Custom Q&A

What is the molecular formula of 5-Bromo-2-iodobenzotrifluoride?

The molecular formula of 5-Bromo-2-iodobenzotrifluoride is C7H3BrF3I.

What is the molecular weight of 5-Bromo-2-iodobenzotrifluoride?

The molecular weight of 5-Bromo-2-iodobenzotrifluoride is 350.90 g/mol.

What is the IUPAC name of 5-Bromo-2-iodobenzotrifluoride?

The IUPAC name of 5-Bromo-2-iodobenzotrifluoride is 4-bromo-1-iodo-2-(trifluoromethyl)benzene.

What is the InChI of 5-Bromo-2-iodobenzotrifluoride?

The InChI of 5-Bromo-2-iodobenzotrifluoride is InChI=1S/C7H3BrF3I/c8-4-1-2-6(12)5(3-4)7(9,10)11/h1-3H.

What is the InChIKey of 5-Bromo-2-iodobenzotrifluoride?

The InChIKey of 5-Bromo-2-iodobenzotrifluoride is FTIZUXGKTNJZEG-UHFFFAOYSA-N.

What is the canonical SMILES of 5-Bromo-2-iodobenzotrifluoride?

The canonical SMILES of 5-Bromo-2-iodobenzotrifluoride is C1=CC(=C(C=C1Br)C(F)(F)F)I.

What is the CAS number of 5-Bromo-2-iodobenzotrifluoride?

The CAS number of 5-Bromo-2-iodobenzotrifluoride is 364-12-5.

What is the European Community (EC) Number of 5-Bromo-2-iodobenzotrifluoride?

The European Community (EC) Number of 5-Bromo-2-iodobenzotrifluoride is 672-496-2.

What is the molecular weight of 5-Bromo-2-iodobenzotrifluoride according to PubChem?

The molecular weight of 5-Bromo-2-iodobenzotrifluoride according to PubChem is 350.90 g/mol.

Is 5-Bromo-2-iodobenzotrifluoride a canonicalized compound according to PubChem?

Yes, 5-Bromo-2-iodobenzotrifluoride is a canonicalized compound according to PubChem.

Synthetic Use

Upstream Synthesis Route 1

• 589-87-7
• 76-05-1

• 364-11-4
• 364-12-5

Reference: [1] Organic Letters, 2015, vol. 17, # 1, p. 38 - 41

Upstream Synthesis Route 2

• 445-02-3

• 364-12-5

Reference: [1] Journal of Medicinal Chemistry, 2014, vol. 57, # 21, p. 9096 - 9104

Upstream Synthesis Route 3

• 401-78-5

• 364-12-5

Reference: [1] Journal of the American Chemical Society, 2008, vol. 130, # 2, p. 472 - 480
[2] Journal of the American Chemical Society, 1951, vol. 73, p. 3932

Upstream Synthesis Route 4

• 445-02-3

• 364-12-5

Reference: [1]Journal of Medicinal Chemistry,2014,vol. 57,p. 9096 - 9104
[2]Tetrahedron Letters,2009,vol. 50,p. 7263 - 7267
[3]Journal of the American Chemical Society,1951,vol. 73,p. 3932
[4]Bioorganic and Medicinal Chemistry,2007,vol. 15,p. 2198 - 2205
[5]Angewandte Chemie - International Edition,2016,vol. 55,p. 10406 - 10409
Angew. Chem.,2016,vol. 128,p. 10562 - 10565,4

Downstream Synthesis Route 1

• 364-12-5

• 401-78-5

Reference: [1]Journal of the Chemical Society. Perkin transactions II,1982,p. 1593 - 1598

Downstream Synthesis Route 2

• 124-38-9
• 364-12-5

• 320-31-0

Reference: [1]Bioorganic and Medicinal Chemistry,2007,vol. 15,p. 2198 - 2205

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