Structure

3,5-Difluoroaniline

CAS
372-39-4
Catalog Number
ACM372394
Category
Aryl Fluorinated Building Blocks
Molecular Weight
129.11
Molecular Formula
C6H5F2N

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Specification

Synonyms
3,5-DIFLUOROBENZENAMINE;3,5-DIFLUOROANILINE;3,5-Difluoroaniline(AntibacterialAntiphlogistic,WeedKiller)(C6H5F2N);3,5-Difluoroaniline,98%;3,5-Difluoroaniline 98%;3,5-DIFLUOROBENZENEAMINE;Benzenamine, 3,5-difluoro;3,5-Difluoronitroaniline
Boiling Point
80°C20mm
Melting Point
37-41°C(lit.)
Flash Point
167°F
Density
1,295 g/cm³
Hazard Statements
Xn,Xi
RIDADR
UN 2941 6.1 / PGIII
Safety Description
28-36/37/39-26-36
Supplemental Hazard Statements
H302-H312-H332-H335-H302+H312+H332-H301+H311+H331-H315-H319
Symbol
GHS06,GHS07
What is the molecular formula of 3,5-Difluoroaniline?

The molecular formula of 3,5-Difluoroaniline is C6H5F2N.

What is the molecular weight of 3,5-Difluoroaniline?

The molecular weight of 3,5-Difluoroaniline is 129.11 g/mol.

What is the IUPAC name of 3,5-Difluoroaniline?

The IUPAC name of 3,5-Difluoroaniline is 3,5-difluoroaniline.

What is the InChI of 3,5-Difluoroaniline?

The InChI of 3,5-Difluoroaniline is InChI=1S/C6H5F2N/c7-4-1-5(8)3-6(9)2-4/h1-3H,9H2.

What is the InChIKey of 3,5-Difluoroaniline?

The InChIKey of 3,5-Difluoroaniline is KQOIBXZRCYFZSO-UHFFFAOYSA-N.

What is the canonical SMILES of 3,5-Difluoroaniline?

The canonical SMILES of 3,5-Difluoroaniline is C1=C(C=C(C=C1F)F)N.

What is the CAS number of 3,5-Difluoroaniline?

The CAS number of 3,5-Difluoroaniline is 372-39-4.

What is the European Community (EC) number of 3,5-Difluoroaniline?

The European Community (EC) number of 3,5-Difluoroaniline is 206-752-8.

What is the UNII of 3,5-Difluoroaniline?

The UNII of 3,5-Difluoroaniline is 93F28C8C0X.

Is 3,5-Difluoroaniline a canonicalized compound?

Yes, 3,5-Difluoroaniline is a canonicalized compound.

Downstream Synthesis Route 1

  • 372-39-4
  • 461-96-1

Reference: [1] Journal of Physical Chemistry A, 2000, vol. 104, # 2, p. 352 - 361

Downstream Synthesis Route 2

  • 372-39-4
  • 2713-34-0

Reference: [1] Journal of the American Chemical Society, 1959, vol. 81, p. 94,95, 97

Downstream Synthesis Route 3

  • 372-39-4
  • 2106-40-3

Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
[3] Journal of the American Chemical Society, 1951, vol. 73, p. 153[4] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98

Downstream Synthesis Route 4

  • 372-39-4
  • 372-38-3
  • 1435-43-4

Reference: [1]Journal of the American Chemical Society,1951,vol. 73,p. 153
Journal of the American Chemical Society,1959,vol. 81,p. 94,98

Downstream Synthesis Route 5

  • 372-39-4
  • 1542-34-3

Reference: [1]Journal of Fluorine Chemistry,2003,vol. 124,p. 39 - 43
[2]Synthetic Communications,2009,vol. 39,p. 1100 - 1108
[3]Journal of Organic Chemistry,1961,vol. 26,p. 3351 - 3356

Downstream Synthesis Route 6

  • 372-39-4
  • 99389-26-1

Reference: [1]Canadian Journal of Chemistry,1985,vol. 63,p. 2471 - 2475
[2]Bioorganic and Medicinal Chemistry Letters,2005,vol. 15,p. 2225 - 2230
[3]Journal of Medicinal Chemistry,1997,vol. 40,p. 2363 - 2373
[4]Patent: WO2013/127267,2013,A1

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

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