2,3-Dichlorobenzaldehyde

Names

[ Name ]:
2,3-Dichlorobenzaldehyde

[Synonym ]:
Benzaldehyde, 2,3-dichloro-
2,3-Dichlorbenzaldehyd
EINECS 228-711-3
2,3-Dichlorobenzaldehyde
2,3,6,7,10,11-HEXAACETOXYTRIPHENYLENE
2,3-dichlorobenzylaldehyde
Benzaldehyde,2,3-dichloro
dichlorobenzaldehyde
2,3-dichloro-benzaldehyde
3,6-dichlorobenzaldehyde
MFCD00010127
2,3-Dichlorobenzalde
2,3-dichloro-benzaldehyd
Benzaldehyde, dichloro-
2,3-diclorobenzaldehyde
2,3-dichlorophenyl aldehyde

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
242.9±20.0 °C at 760 mmHg

[ Melting Point ]:
64-67 °C(lit.)

[ Molecular Formula ]:
C₇H₄Cl₂O

[ Molecular Weight ]:
175.012

[ Flash Point ]:
99.2±22.3 °C

[ Exact Mass ]:
173.963913

[ PSA ]:
17.07000

[ LogP ]:
2.82

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.601

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36/37/39-S45-S37/39

[ RIDADR ]:
UN 3261 8/PG 2

[ WGK Germany ]:
2

[ Packaging Group ]:
III

[ Hazard Class ]:
8

[ HS Code ]:
29130000

Synthetic Route

Click to get detail synthetic route

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

4-(2, 3-Dichlorobenzylideneamino)-1, 5-dimethyl-2-phenyl-1H-pyrazol-3 (2H)-one. Sun, Y-X., et al.

Acta Crystallogr. Sect. E Struct. Rep. Online 62(10) , o4613-15, (2006)

Synthesis and reactions of Biginelli-compounds. Part 23.1 Chemoenzymatic syntheses of enantiomerically pure 4-aryl-3, 4-dihydropyrimidin-2 (1H)-ones. Schnell B, et al.

J. Chem. Soc. Perkin Trans. I 24 , 4382-89, (2000)