5-Fluoro-2-hydroxybenzaldehyde

Names

[ CAS No. ]:
347-54-6

[ Name ]:
5-Fluoro-2-hydroxybenzaldehyde

[Synonym ]:
VHR BQ EF
5-fluoro-2-hydroxy-benzaldehyde
2-hydroxy-5-fluorobenzaldehyde
MFCD01090997
Benzaldehyde, 5-fluoro-2-hydroxy-
5-Fluoro-2-hydroxybenzaldehyde
5-Fluorosalicylaldehyde
4-fluoro-2-formylphenol
5-fluorosalicyclaldehyde

Biological Activity

[Description]:

5-Fluoro-2-hydroxybenzaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
207.4±20.0 °C at 760 mmHg

[ Melting Point ]:
82-85 °C(lit.)

[ Molecular Formula ]:
C₇H₅FO₂

[ Molecular Weight ]:
140.11

[ Flash Point ]:
79.2±21.8 °C

[ Exact Mass ]:
140.027359

[ PSA ]:
37.30000

[ LogP ]:
2.10

[ Vapour Pressure ]:
0.2±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.587

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2913000090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2913000090

[ Summary ]:
HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%

Articles

Large perturbations of long-range n J (1H, 1H) and n J (1H, 19F) by the intramolecular hydrogen bonds in 2-mercaptobenzaldehyde, salicylaldehyde, and some derivatives. Reference structures for intramolecular hydrogen bonds. Schaefer T, et al.

Can. J. Chem. 71(7) , 960-967, (1993)

Manganese (III) complexes derived from bis-Schiff bases: Synthesis, structures, and antimicrobial activity. Liu QR, et al.

Russ. J. Coord. Chem. 40(10) , 757-763, (2014)

Synthesis of Enantiopure 4-Amino-6-fluoro-3-(hydroxymethyl) chromanes via Intramolecular Nitrone Cycloadditions. Broggini G, et al.

J. Chem. Res. Synop. 2 , 36-37, (1997)