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653586

4-Fluoro-1,2-phenylenediamine

97%

Synonym(s):

1,2-Diamino-4-fluorobenzene, 4-Fluoro-o-phenylenediamine

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About This Item

Empirical Formula (Hill Notation):
C6H7FN2
CAS Number:
367-31-7
Molecular Weight:
126.13
Beilstein/REAXYS Number:
2081075
EC Number:
206-691-7
MDL number:
MFCD00042228
UNSPSC Code:
12352100
PubChem Substance ID:
24883967
NACRES:
NA.22

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Quality Level

200

assay

97%

mp

94-98 °C

functional group

fluoro

SMILES string

Nc1ccc(F)cc1N

InChI

1S/C6H7FN2/c7-4-1-2-5(8)6(9)3-4/h1-3H,8-9H2

InChI key

KWEWNOOZQVJONF-UHFFFAOYSA-N

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This Item
F3800D71607191760
4-Fluoro-1,2-phenylenediamine 97%

Sigma-Aldrich

653586

4-Fluoro-1,2-phenylenediamine

4-Fluoroaniline 99%

Sigma-Aldrich

F3800

4-Fluoroaniline

4,5-Dichloro-o-phenylenediamine 97%

Sigma-Aldrich

D71607

4,5-Dichloro-o-phenylenediamine

3,4-Diaminobenzophenone 97%

Sigma-Aldrich

191760

3,4-Diaminobenzophenone

assay

97%

assay

99%

assay

97%

assay

97%

mp

94-98 °C

mp

-

mp

158-164 °C (lit.)

mp

115-117 °C (lit.)

functional group

fluoro

functional group

-

functional group

-

functional group

-

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000508691
0000508691
0000475541
0000475541
0000382217

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Andreas Kiontke et al.
Analytical and bioanalytical chemistry, 410(16), 3715-3722 (2018-04-14)
Ambient ionization mass spectrometry (AI-MS), the ionization of samples under ambient conditions, enables fast and simple analysis of samples without or with little sample preparation. Due to their simple construction and low resource consumption, plasma-based ionization methods in particular are
Anshul Singh et al.
Bioinorganic chemistry and applications, 2018, 2467463-2467463 (2018-06-01)
We present an inclusive characterization of the unimetallic and heterobimetallic complexes of copper synthesized using CuCl2 and diamine (4-fluoro 1,2-phenylenediamine) resulting in monometallic complex which further undergoes treatment with organometallic dichlorides of group 4 and 14 in 1 : 2 molar ratio

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