70738-05-5

Basic information

• Product Name: Benzaldehyde, 3,6-dihydroxy-2-iodo-
• CAS NO: 70738-05-5
• Molecular Formula: C7H5IO3
• Molecular Weight: 264.019
• Mol File: 70738-05-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 3,6-dihydroxy-2-iodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 3,6-dihydroxy-2-iodo-(70738-05-5)
• EPA Substance Registry System: Benzaldehyde, 3,6-dihydroxy-2-iodo-(70738-05-5)

Safety Data

• Hazardous Substances Data: 70738-05-5(Hazardous Substances Data)

Upstream product

• 71255-05-5 2-iodo-3,6-dimethoxybenzyl vinyl ether 
• 71255-03-3 2,5-dimethoxybenzyl vinyl ether 
• 71255-06-6 2-iodo-3,6-dimethoxybenzyl alcohol 
• 33524-31-1 2,5-dimethoxybenzyl alcohol 
• 70738-04-4 2-iodo-3,6-dimethoxybenzaldehyde 

Downstream Products

• 63160-44-1 2-hydroxymethyl-3-(3-methylbut-3-en-1-ynyl)benzene-1,4-diol 
• 63160-46-3 2,5-dihydroxy-6-(3-methylbut-3-en-1-ynyl)benzaldehyde 
• 73151-59-4 (7E,9E,11E)-aurocitrin 
• 81477-64-7 3-O-(tert-butyldimethylsilyl)frustulosin 
• 81477-68-1 2-iodo-3,6-bis<(tert-butyldimethylsilyl)oxy>cinnamaldehyde 
• 81477-63-6 bis(tert-butyldimethylsilyl)frustulosin 
• 81477-70-5 5-<2-iodo-3,6-bis(tert-butyldimethylsiloxy)phenyl>-2,4-pentadienal 
• 81477-65-8 1-<2-iodo-3,6-bis(tert-butyldimethylsiloxy)phenyl>-1,3,5-undecatriene 
• 81477-71-6 1-<2-iodo-3,6-bis(tert-butyldimethylsiloxy)phenyl>-1,3-undecadien-5-ol 
• 81477-62-5 2-iodo-3-<(tert-butyldimethylsilyl)oxy>-6-hydroxybenzaldehyde 
• 81477-60-3 3-isopropenyl-4-formyl-5-hydroxybenzofuran 

Relevant articles and documents

Total Synthesis of Frustulosin and Aurocitrin

The regioselective total syntheses of the novel fungal antibiotics frustulosin (1) and aurocitrin (2) were accomplished from 3,6-dihydroxy-2-iodobenzaldehyde (10) which was prepared by a regiodirected metalation of 2,5-dimethylbenzyl vinyl ether to establish the 1,2,3,4-tetrasubstitution pattern of these compounds.The unsaturated side chains of these hydroquinone antibiotics were attached by using the iodo aldehyde functionalities.The structures of these antibiotics are confirmed by synthesis.