71255-03-3

Basic information

• Product Name: Benzene, 2-[(ethenyloxy)methyl]-1,4-dimethoxy-
• Synonyms: 1,4-Dimethoxy-2-[(vinyloxy)methyl]benzene;Benzene,2-[(ethenyloxy)methyl]-1,4-dimethoxy;2,5-dimethoxybenzyl vinyl ether
• CAS NO: 71255-03-3
• Molecular Formula: C11H14O3
• Molecular Weight: 194.23
• Mol File: 71255-03-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 288.2±30.0 °C(Predicted)
• Density: 1.031±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzene, 2-[(ethenyloxy)methyl]-1,4-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-[(ethenyloxy)methyl]-1,4-dimethoxy-(71255-03-3)
• EPA Substance Registry System: Benzene, 2-[(ethenyloxy)methyl]-1,4-dimethoxy-(71255-03-3)

Safety Data

• Hazardous Substances Data: 71255-03-3(Hazardous Substances Data)

Upstream product

• 33524-31-1 2,5-dimethoxybenzyl alcohol 
• 109-92-2 ethyl vinyl ether 

Downstream Products

• 87850-30-4 3,6-Dimethoxy-2-vinyloxymethyl-benzaldehyde 
• 81477-71-6 1-<2-iodo-3,6-bis(tert-butyldimethylsiloxy)phenyl>-1,3-undecadien-5-ol 
• 81477-65-8 1-<2-iodo-3,6-bis(tert-butyldimethylsiloxy)phenyl>-1,3,5-undecatriene 
• 81477-70-5 5-<2-iodo-3,6-bis(tert-butyldimethylsiloxy)phenyl>-2,4-pentadienal 
• 81477-63-6 bis(tert-butyldimethylsilyl)frustulosin 
• 81477-68-1 2-iodo-3,6-bis<(tert-butyldimethylsilyl)oxy>cinnamaldehyde 
• 81477-61-4 2-iodo-3,6-bis<(tert-butyldimethylsilyl)oxy>benzaldehyde 
• 81477-64-7 3-O-(tert-butyldimethylsilyl)frustulosin 
• 81477-62-5 2-iodo-3-<(tert-butyldimethylsilyl)oxy>-6-hydroxybenzaldehyde 
• 73151-59-4 (7E,9E,11E)-aurocitrin 
• 71255-06-6 2-iodo-3,6-dimethoxybenzyl alcohol 
• 70738-04-4 2-iodo-3,6-dimethoxybenzaldehyde 
• 70738-05-5 2-iodo-3,6-dihydrobenzaldehyde 
• 63160-46-3 2,5-dihydroxy-6-(3-methylbut-3-en-1-ynyl)benzaldehyde 

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.