4-Nitro-2-(trifluoromethyl)aniline

• CAS: 121-01-7
• Catalog Number: ACM121017
• Category: Amines
• Molecular Weight: 206.12
• Molecular Formula: C₇H₅Cl₂NO₂
• Hazard Statements: H302-H317-H319
• RIDADR: NONH for all modes of transport
• Symbol: GHS07

Custom Q&A

What is the molecular weight of 4-Nitro-2-(trifluoromethyl)aniline?

The molecular weight of 4-Nitro-2-(trifluoromethyl)aniline is 206.12 g/mol.

What is the IUPAC name of 4-Nitro-2-(trifluoromethyl)aniline?

The IUPAC name of 4-Nitro-2-(trifluoromethyl)aniline is 4-nitro-2-(trifluoromethyl)aniline.

What is the InChIKey of 4-Nitro-2-(trifluoromethyl)aniline?

The InChIKey of 4-Nitro-2-(trifluoromethyl)aniline is HOTZLWVITTVZGY-UHFFFAOYSA-N.

How many hydrogen bond donor counts does 4-Nitro-2-(trifluoromethyl)aniline have?

4-Nitro-2-(trifluoromethyl)aniline has 1 hydrogen bond donor count.

What is the exact mass of 4-Nitro-2-(trifluoromethyl)aniline?

The exact mass of 4-Nitro-2-(trifluoromethyl)aniline is 206.03031189 g/mol.

How many hydrogen bond acceptor counts does 4-Nitro-2-(trifluoromethyl)aniline have?

4-Nitro-2-(trifluoromethyl)aniline has 6 hydrogen bond acceptor counts.

What is the topological polar surface area of 4-Nitro-2-(trifluoromethyl)aniline?

The topological polar surface area of 4-Nitro-2-(trifluoromethyl)aniline is 71.8 Ų.

How many rotatable bond counts does 4-Nitro-2-(trifluoromethyl)aniline have?

4-Nitro-2-(trifluoromethyl)aniline has 0 rotatable bond counts.

Is 4-Nitro-2-(trifluoromethyl)aniline a covalently-bonded unit?

Yes, 4-Nitro-2-(trifluoromethyl)aniline is a covalently-bonded unit.

What is the complexity of 4-Nitro-2-(trifluoromethyl)aniline?

The complexity of 4-Nitro-2-(trifluoromethyl)aniline is 226.

Synthetic Use

Upstream Synthesis Route 1

• 98-46-4

• 121-01-7
• 400-98-6

Reference: [1] Journal of Organic Chemistry, 1998, vol. 63, # 15, p. 4878 - 4888

Upstream Synthesis Route 2

• 98-46-4

• 121-01-7
• 24821-17-8
• 400-98-6

Reference: [1] Journal of Organic Chemistry, 1996, vol. 61, # 2, p. 442 - 443
[2] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 11, p. 1437 - 1444

Upstream Synthesis Route 3

• 777-37-7

• 121-01-7

Reference: [1] Tetrahedron, 2010, vol. 66, # 38, p. 7642 - 7650
[2] Patent: US2194926, 1937, ,
[3] Journal of Organic Chemistry, 1961, vol. 26, p. 2707 - 2710
[4] Journal of Organic Chemistry, 1962, vol. 27, p. 4660 - 4662

Downstream Synthesis Route 1

• 1930-72-9
• 121-01-7

• 53446-58-5

Reference: [1]Patent: FR2211450,1974,

Downstream Synthesis Route 2

• 121-01-7
• 2401-85-6

• 68105-51-1

Reference: [1]Patent: DE2708440,1978,

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