100866-04-4

Basic information

• Product Name: [3-iodo-4-(4-methoxy-phenoxy)-phenyl]-acetonitrile
• Synonyms: [3-iodo-4-(4-methoxy-phenoxy)-phenyl]-acetonitrile
• CAS NO: 100866-04-4
• Molecular Weight: 365.17
• Mol File: 100866-04-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [3-iodo-4-(4-methoxy-phenoxy)-phenyl]-acetonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: [3-iodo-4-(4-methoxy-phenoxy)-phenyl]-acetonitrile(100866-04-4)
• EPA Substance Registry System: [3-iodo-4-(4-methoxy-phenoxy)-phenyl]-acetonitrile(100866-04-4)

Safety Data

• Hazardous Substances Data: 100866-04-4(Hazardous Substances Data)

Upstream product

• 1304495-15-5 C₁₅H₁₄N₂O₂ 
• 459-22-3 4-fluorophenylacetonitrile 
• 446-11-7 4-fluoro-3-nitrotoluene 
• 15017-52-4 4-(bromomethyl)-1-fluoro-2-nitrobenzene 
• 157662-77-6 2-(4-fluoro-3-nitrophenyl)acetonitrile 
• 20274-70-8 4-(chloromethyl)-1-fluoro-2-nitrobenzene 
• 140-53-4 p-chlorobenzyl cyanide 
• 3360-45-0 4-chloro-3-nitro-benzylbromide 
• 57403-35-7 1-chloro-4-(chloromethyl)-2-nitrobenzene 
• 89-60-1 1-chloro-4-methyl-2-nitro-benzene 
• 55912-20-4 4-chloro-3-nitrobenzyl alcohol 
• 51250-90-9 2-(4-chloro-3-nitrophenyl)acetonitrile 
• 100717-19-9 3-iodo-4-(4-methoxy-phenoxy)-benzyl alcohol 
• 100542-63-0 1-(4-chloromethyl-2-iodo-phenoxy)-4-methoxy-benzene 

Downstream Products

• 788824-56-6 N-t-butoxycarbonyl-3-iodothyronamine 
• 788824-64-6 3-Iodothyronamine hydrochloride 
• 1304495-16-6 C₁₄H₁₀INO₂ 
• 92151-30-9 3,3′,5-tetraiodothyroacetic acid 
• 121-26-6 [4-(4-hydroxy-3-iodo-phenoxy)-3-iodo-phenyl]-acetic acid 
• 60578-17-8 3-iodothyroacetic acid 
• 101096-67-7 [3-iodo-4-(4-methoxy-phenoxy)-phenyl]-acetic acid 

Relevant articles and documents

A new efficient synthetic method for 3-iodothyronamine and its potent hypothermic efficacy

We developed a new efficient synthetic method for a 3-iodothyronamine (T1AM) that has advantages of less synthetic steps and much higher overall yield compared to those in the conventional method. Our animal study showed that T1AM synthesized by the method exerted a potent hypothermic effect in non-hibernator mice.