2-Fluorobenzoic hydrazide

• CAS: 446-24-2
• Catalog Number: ACM446242
• Category: Aryl Fluorinated Building Blocks
• Molecular Weight: 154.14
• Molecular Formula: C₇H₇ClFN
• Hazard Statements: H302-H315-H319
• RIDADR: NONH for all modes of transport
• Symbol: GHS07

Custom Q&A

What is the molecular formula of 2-Fluorobenzoic hydrazide?

The molecular formula is C7H7FN2O.

When was 2-Fluorobenzoic hydrazide first created?

It was first created on 2005-03-26.

What is the IUPAC name of 2-Fluorobenzoic hydrazide?

The IUPAC name is 2-fluorobenzohydrazide.

What is the InChI of 2-Fluorobenzoic hydrazide?

The InChI is InChI=1S/C7H7FN2O/c8-6-4-2-1-3-5(6)7(11)10-9/h1-4H,9H2,(H,10,11).

What is the molecular weight of 2-Fluorobenzoic hydrazide?

The molecular weight is 154.14 g/mol.

How many hydrogen bond donor counts does 2-Fluorobenzoic hydrazide have?

It has 2 hydrogen bond donor counts.

What is the topological polar surface area of 2-Fluorobenzoic hydrazide?

The topological polar surface area is 55.1 Ų.

Is 2-Fluorobenzoic hydrazide a canonicalized compound?

Yes, it is a canonicalized compound.

What is the CAS number of 2-Fluorobenzoic hydrazide?

The CAS number is 446-24-2.

How many rotatable bond counts does 2-Fluorobenzoic hydrazide have?

It has 1 rotatable bond count.

Synthetic Use

Upstream Synthesis Route 1

• 443-26-5

• 446-24-2

Reference: [1] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 17, p. 6014 - 6024

Upstream Synthesis Route 2

• 394-35-4

• 446-24-2

Reference: [1] Patent: WO2011/5520, 2011, A1, . Location in patent: Page/Page column 31

Upstream Synthesis Route 3

• 393-52-2

• 446-24-2

Reference: [1] Chemistry of Heterocyclic Compounds, 2005, vol. 41, # 12, p. 1511 - 1520

Upstream Synthesis Route 4

• 443-26-5

• 446-24-2

Reference: [1]Bioorganic and Medicinal Chemistry,2015,vol. 23,p. 6014 - 6024

Upstream Synthesis Route 5

• 445-28-3

• 446-24-2

Reference: [1]Chemische Berichte,1937,vol. 70,p. 1416,1419

Downstream Synthesis Route 1

• 446-24-2
• 556-61-6

• 116850-73-8

Reference: [1]Kane; Staeger; Dalton; Miller; Dudley; Ogden; Kehne; Ketteler; McCloskey; Senyah; Chmielewski; Miller
[Journal of Medicinal Chemistry, 1994, vol. 37, # 1, p. 125 - 132]
[2]Kane, John M.; Dalton, Christopher R.; Staeger, Michael A.; Huber, Edward W.
[Journal of Heterocyclic Chemistry, 1995, vol. 32, # 1, p. 183 - 188]

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