129488
5-Iodovanillin
97%
Synonym(s):
4-Hydroxy-3-iodo-5-methoxybenzaldehyde
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
IC6H2(OCH3)(OH)CHO
CAS Number:
Molecular Weight:
278.04
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
powder
mp
183-185 °C (lit.)
SMILES string
COc1cc(C=O)cc(I)c1O
InChI
1S/C8H7IO3/c1-12-7-3-5(4-10)2-6(9)8(7)11/h2-4,11H,1H3
InChI key
FBBCSYADXYILEH-UHFFFAOYSA-N
Related Categories
Application
5-Lodovanillin was used in the characterization of 5-Iodoacetovanillone. 5-Iodovanillin has also been used in the synthesis of platelet activating factor antagonist L-659,989.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
An improved synthesis of acetosyringone.
Crawford LW, et al.
Canadian Journal of Chemistry, 34(11), 1562-1566 (1956)
Thompson AS, et al.
Tetrahedron Letters, 31(48), 6953-6956 (1990)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service