3-Fluorobenzyl chloride

• CAS: 456-42-8
• Catalog Number: ACM456428
• Category: Aryl
• Molecular Weight: 144.57
• Hazard Statements: H315-H319-H335
• RIDADR: UN 3261 8 / PGII
• Symbol: GHS07

Custom Q&A

What is the molecular formula of 3-Fluorobenzyl chloride according to the reference?

The molecular formula of 3-Fluorobenzyl chloride is C7H6ClF.

What is the molecular weight of 3-Fluorobenzyl chloride?

The molecular weight of 3-Fluorobenzyl chloride is 144.57 g/mol.

What is the IUPAC name of 3-Fluorobenzyl chloride?

The IUPAC name of 3-Fluorobenzyl chloride is 1-(chloromethyl)-3-fluorobenzene.

What is the InChIKey of 3-Fluorobenzyl chloride?

The InChIKey of 3-Fluorobenzyl chloride is XBDXMDVEZLOGMC-UHFFFAOYSA-N.

How many hydrogen bond acceptor counts does 3-Fluorobenzyl chloride have?

3-Fluorobenzyl chloride has 1 hydrogen bond acceptor count.

What is the topological polar surface area of 3-Fluorobenzyl chloride?

The topological polar surface area of 3-Fluorobenzyl chloride is 0Ų.

Is 3-Fluorobenzyl chloride a covalently-bonded unit?

Yes, 3-Fluorobenzyl chloride is a covalently-bonded unit.

What is the CAS number of 3-Fluorobenzyl chloride?

The CAS number of 3-Fluorobenzyl chloride is 456-42-8.

How many rotatable bond counts does 3-Fluorobenzyl chloride have?

3-Fluorobenzyl chloride has 1 rotatable bond count.

What is the formal charge of 3-Fluorobenzyl chloride?

The formal charge of 3-Fluorobenzyl chloride is 0.

Synthetic Use

Upstream Synthesis Route 1

• 352-70-5

• 456-42-8

Reference: [1] Journal of the Chemical Society, 1949, p. 1089,1096

Upstream Synthesis Route 2

• 65108-06-7

• 456-42-8

Reference: [1] Journal of the American Chemical Society, 1985, vol. 107, # 13, p. 3747 - 3757

Upstream Synthesis Route 3

• 352-70-5

• 456-42-8

Reference: [1]Journal of Fluorine Chemistry,2019,vol. 226

Downstream Synthesis Route 1

• 456-42-8

• 456-41-7

Reference: [1] Journal of the American Chemical Society, 1980, vol. 102, # 4, p. 1367 - 1371
[2] Nippon Kagaku Zasshi, 1958, vol. 79, p. 1428,1430[3] Chem.Abstr., 1960, p. 5518

Downstream Synthesis Route 2

• 56-40-6
• 456-42-8

• 19883-77-3

Reference: [1]Ghalehbandi, Shermineh sadat; Ghazanfari, Dadkhoda; Ahmadi, Sayed Ali; Sheikhhosseini, Enayatollah
[Organic Preparations and Procedures International, 2021, vol. 53, # 2, p. 176 - 183]
[2]Wang, Jingjing; Zhai, Yongyan; Wang, Ying; Yu, Han; Zhao, Wenshu; Wei, Yongge
[Dalton Transactions, 2018, vol. 47, # 38, p. 13323 - 13327]
[3]Yu, Han; Wang, Jingjing; Zhai, Yongyan; Zhang, Mengqi; Ru, Shi; Han, Sheng; Wei, Yongge
[ChemCatChem, 2018, vol. 10, # 19, p. 4274 - 4279]
[4]Baker; Hopkins
[Journal of the Chemical Society, 1949, p. 1089,1096]

Downstream Synthesis Route 3

• 23795-02-0
• 456-42-8

• 56442-27-4

Reference: [1]Bulletin of the Academy of Sciences of the USSR Division of Chemical Science,1990,vol. 39,p. 1479 - 1485
Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya,1990,p. 1630 - 1636

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