3-Iodo-4,5-dimethoxybenzaldehyde
Names
[ CAS No. ]:
32024-15-0
[ Name ]:
3-Iodo-4,5-dimethoxybenzaldehyde
[Synonym ]:
4,5-Dimethoxy-3-iodobenzaldehyde
5-iodo-3,4-dimethoxybenzaldehyde
3-iodo-4,5-dimethoxy-benzaldehyde
MFCD00674091
3-Iodo-4,5-dimethoxybenzaldehyde
3-Jod-4,5-dimethoxy-benzaldehyd
3,4-dimethoxy-5-iodo-benzaldehyde
Benzaldehyde, 3-iodo-4,5-dimethoxy-
5-iodo veratryl aldehyde
Chemical & Physical Properties
[ Density]:
1.7±0.1 g/cm3
[ Boiling Point ]:
362.7±42.0 °C at 760 mmHg
[ Melting Point ]:
63-65°C
[ Molecular Formula ]:
C9H9IO3
[ Molecular Weight ]:
292.070
[ Flash Point ]:
173.2±27.9 °C
[ Exact Mass ]:
291.959625
[ PSA ]:
35.53000
[ LogP ]:
2.74
[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C
[ Index of Refraction ]:
1.609
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
[ HS Code ]:
2913000090
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
J. Nat. Prod. 75(3) , 385-93, (2012)
Toward the objective of designing a structurally modified analogue of the combretastatin A-4 phosphate prodrug (1b) with the potential for increased specificity toward thyroid carcinoma, synthesis of ...
Total synthesis of chloropeptin II (complestatin) and chloropeptin I.J. Am. Chem. Soc. 131(44) , 16036-8, (2009)
The first total synthesis of chloropeptin II (1, complestatin) is disclosed. Key elements of the approach include the use of an intramolecular Larock indole synthesis for the initial macrocyclization,...
Nucleophilic catalysis of the iodine-zinc exchange reaction: preparation of highly functionalized diaryl zinc compounds.Angew. Chem. Int. Ed. Engl. 43(8) , 1017-21, (2004)