Basic information Safety Supplier Related

3-IODO-4-METHOXY-BENZALDEHYDE

Basic information Safety Supplier Related

3-IODO-4-METHOXY-BENZALDEHYDE Basic information

Product Name:
3-IODO-4-METHOXY-BENZALDEHYDE
Synonyms:
  • 3-IODO-4-METHOXY-BENZALDEHYDE
  • 3-Iodo-p-anisaldehyde, 4-Formyl-2-iodoanisole
  • 3-Iodo-4-methoxybenzaldehyde 97%
  • Benzaldehyde, 3-iodo-4-methoxy-
CAS:
2314-37-6
MF:
C8H7IO2
MW:
262.04
Product Categories:
  • aldehyde| alkyl Iodine
  • Adehydes, Acetals & Ketones
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Iodine Compounds
Mol File:
2314-37-6.mol
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3-IODO-4-METHOXY-BENZALDEHYDE Chemical Properties

Melting point:
107-112℃
Boiling point:
325.0±32.0 °C(Predicted)
Density 
1.780±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
Solid
color 
White to off-white/yellow
Sensitive 
Air & Light Sensitive
InChI
InChI=1S/C8H7IO2/c1-11-8-3-2-6(5-10)4-7(8)9/h2-5H,1H3
InChIKey
RVWOHBWQJGLXIJ-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=C(OC)C(I)=C1
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Safety Information

Hazard Codes 
Xn,N
Risk Statements 
22-50
Safety Statements 
61
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
HazardClass 
6.1
HS Code 
2912290090
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3-IODO-4-METHOXY-BENZALDEHYDE Usage And Synthesis

Synthesis

123-11-5

2314-37-6

General procedure for the synthesis of compounds (CAS:2314-37-6) from p-methoxybenzaldehyde: To a solution (0.1 M) of dichloromethane (CH2Cl2) or 1,2-dichloroethane ((CH2Cl)2) in stirring (1 mmol) of the substrate (1 mmol), Ph3PAuNTf2 (0.025 mmol, 19 mg; if using the 2:1 complex of Ph3PAuNTf2 with toluene), followed by N-iodosuccinimide (1.1 mmol, 248 mg). The reaction mixture was stirred at room temperature or reacted under reflux conditions until complete conversion of the feedstock. Upon completion of the reaction, the solvent was removed under reduced pressure and the crude product was purified by fast column chromatography using different ratios of hexane and ethyl acetate (EtOAc) as eluents to give the final pure target product.

References

[1] European Journal of Organic Chemistry, 2000, # 8, p. 1527 - 1533
[2] European Journal of Organic Chemistry, 2012, # 30, p. 5935 - 5942,8
[3] Synthesis, 2010, # 16, p. 2776 - 2786
[4] Organic letters, 2003, vol. 5, # 4, p. 415 - 418
[5] Tetrahedron Letters, 1997, vol. 38, # 35, p. 6305 - 6306

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