4-Iodobenzaldehyde

Names

[ CAS No. ]:
15164-44-0

[ Name ]:
4-Iodobenzaldehyde

[Synonym ]:
Benzaldehyde, 4-iodo-
p-Iodobenzaldehyde
VHR DI
MFCD00039576
4-Iodobenzaldehyde

Chemical & Physical Properties

[ Density]:
1.9±0.1 g/cm3

[ Boiling Point ]:
264.8±23.0 °C at 760 mmHg

[ Melting Point ]:
78-82 °C(lit.)

[ Molecular Formula ]:
C₇H₅IO

[ Molecular Weight ]:
232.02

[ Flash Point ]:
114.0±22.6 °C

[ Exact Mass ]:
231.938507

[ PSA ]:
17.07000

[ LogP ]:
2.83

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

[ Index of Refraction ]:
1.668

[ Storage condition ]:
Keep Cold

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

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

4-Formylphenylboronic acid
4-iodobenzyl alcohol
4-Iodobenzoic acid
1,4-Diiodobenzene
N,N-Dimethylformamide
p-Tolyl sulfoxide (8CI)
4-Iodotoluene
2-(4-iodophenyl)-5,5-dimethyl-[1,3]dioxane
carbon monoxide

DownStream

[1,1',4',1",4",1"'-Quaterphenyl]-4,4'''-dicarbonaldehyde
4-iodocinnamic acid
4-(Trifluoromethyl)benzaldehyde
(E)-tert-Butyl 3-(4-formylphenyl)acrylate
4-Fluorobenzaldehyde
4-iodobenzyl alcohol
N-(4-iodobenzyl)-1,2,3,4-tetrahydroquinaldine
tetrahydroquinaldine
1-iodo-4-(2-phenylethynyl)benzene
1-(4-iodophenyl)propan-2-amine

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

Growth of Thin, Anisotropic, π-Conjugated Molecular Films by Stepwise "Click" Assembly of Molecular Building Blocks: Characterizing Reaction Yield, Surface Coverage, and Film Thickness versus Addition Step Number.

J. Am. Chem. Soc. 137 , 8819-28, (2015)

We report the systematic characterization of anisotropic, π-conjugated oligophenyleneimine (OPI) films synthesized using stepwise imine condensation, or "click" chemistry. Film synthesis began with a ...

Selective cleavage of the carbon-halide bond in substituted benzaldimine monolayers by synchrotron soft X-ray: Anomalously large cleavage rate of the carbon-bromide bond. Moon JH, et al.

Langmuir 16(6) , 2981-84, (2000)

Trans-Substituted porphyrin building blocks bearing iodo and ethynyl groups for applications in bioorganic and materials chemistry. Ravikanth M, et al.

Tetrahedron 54(27) , 7721-34, (1998)