4-Fluorobenzyl chloride

• CAS: 352-11-4
• Catalog Number: ACM352114
• Category: Aryl
• Molecular Weight: 144.57
• Hazard Statements: H314-H334
• RIDADR: UN 2920 3(8) / PGII
• Symbol: GHS05

Custom Q&A

What is the molecular formula of 4-Fluorobenzyl chloride?

The molecular formula of 4-Fluorobenzyl chloride is C7H6ClF.

What is the molecular weight of 4-Fluorobenzyl chloride?

The molecular weight of 4-Fluorobenzyl chloride is 144.57 g/mol.

What is the IUPAC name of 4-Fluorobenzyl chloride?

The IUPAC name of 4-Fluorobenzyl chloride is 1-(chloromethyl)-4-fluorobenzene.

What is the InChI of 4-Fluorobenzyl chloride?

The InChI of 4-Fluorobenzyl chloride is InChI=1S/C7H6ClF/c8-5-6-1-3-7(9)4-2-6/h1-4H,5H2.

What is the InChIKey of 4-Fluorobenzyl chloride?

The InChIKey of 4-Fluorobenzyl chloride is IZXWCDITFDNEBY-UHFFFAOYSA-N.

What is the canonical SMILES of 4-Fluorobenzyl chloride?

The canonical SMILES of 4-Fluorobenzyl chloride is C1=CC(=CC=C1CCl)F.

What is the CAS number of 4-Fluorobenzyl chloride?

The CAS number of 4-Fluorobenzyl chloride is 352-11-4.

What is the European Community (EC) number of 4-Fluorobenzyl chloride?

The European Community (EC) number of 4-Fluorobenzyl chloride is 206-516-4.

What is the DSSTox Substance ID of 4-Fluorobenzyl chloride?

The DSSTox Substance ID of 4-Fluorobenzyl chloride is DTXSID7059850.

Is 4-Fluorobenzyl chloride a compound with defined bond stereocenter count?

No, 4-Fluorobenzyl chloride does not have a defined bond stereocenter count.

Synthetic Use

Downstream Synthesis Route 1

• 352-11-4

• 459-46-1

Reference: [1] Nippon Kagaku Zasshi, 1958, vol. 79, p. 1428,1430[2] Chem.Abstr., 1960, p. 5518

Downstream Synthesis Route 2

• 352-11-4

• 459-31-4

Reference: [1] Journal of Physical Organic Chemistry, 1999, vol. 12, # 10, p. 751 - 757

Downstream Synthesis Route 3

• 352-11-4

• 459-22-3

Reference: [1] Tetrahedron Letters, 2011, vol. 52, # 39, p. 5107 - 5109
[2] Tetrahedron Letters, 2012, vol. 53, # 23, p. 2825 - 2827

Downstream Synthesis Route 4

• 272-14-0
• 352-11-4

• 55142-84-2

Reference: [1]European Journal of Medicinal Chemistry,1974,vol. 9,p. 483 - 486

Downstream Synthesis Route 5

• 4054-67-5
• 352-11-4

• 101161-35-7

Reference: [1]Sudakow, Alex; Jones, Peter G.; Lindel, Thomas
[European Journal of Organic Chemistry, 2012, # 4, p. 681 - 684]
[2]Chatterjee, Tanmay; Kumar, N. Tanmaya; Das, Samar K.
[Polyhedron, 2017, vol. 127, p. 68 - 83]
[3]Carr, Albert A.; Hay, David A.; Kane, John M.; Staeger, Michael A.
[Journal of Organic Chemistry, 1990, vol. 55, # 4, p. 1399 - 1401]
[4]Maynard, George D.; Bratton, Larry D.; Kane, John M.; Burkholder, Timothy P.; Santiago, Braulio; Stewart, Kenneth T.; Kudlacz, Elizabeth M.; Shatzer, Scott A.; Knippenberg, Robert W.; Farrell, Amy M.; Logan, Deborah E.
[Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 22, p. 2819 - 2824]
[5]Current Patent Assignee: SANOFI - US4908372, 1990, A

Downstream Synthesis Route 6

• 603-35-0
• 352-11-4

• 3462-95-1

Reference: [1]Chemical and Pharmaceutical Bulletin,1985,vol. 33,p. 2535 - 2540

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