146197-51-5

Basic information

• Product Name: 3-iodo-2-methylbenzyl methoxymethyl ether
• Synonyms: 3-iodo-2-methylbenzyl methoxymethyl ether
• CAS NO: 146197-51-5
• Molecular Weight: 292.117
• Mol File: 146197-51-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-iodo-2-methylbenzyl methoxymethyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 3-iodo-2-methylbenzyl methoxymethyl ether(146197-51-5)
• EPA Substance Registry System: 3-iodo-2-methylbenzyl methoxymethyl ether(146197-51-5)

Safety Data

• Hazardous Substances Data: 146197-51-5(Hazardous Substances Data)

Upstream product

• 52130-17-3 3-amino-2-methylbenzoic acid 
• 133232-56-1 3-iodo-2-methylbenzoic acid 
• 1975-50-4 2-methyl-3-nitrobenzic acid 
• 107-30-2 chloromethyl methyl ether 
• 76350-89-5 (3-iodo-2-methylphenyl)methanol 
• 109-87-5 Dimethoxymethane 

Downstream Products

• 146197-53-7 4-(3-methoxymethoxymethyl-2-methylbenzoyl)-1-triphenylmethylimidazole 
• 146197-54-8 4-(3-methoxymethoxymethyl-2-methylbenzyl)-1-triphenylmethylimidazole 
• 146197-56-0 methyl 3-(4⁽⁵⁾-imidazolylmethyl)-2-methylbenzoate 
• 115664-37-4 3-(4⁽⁵⁾-imidazolylmethyl)-2-methylbenzyl alcohol 
• 146197-55-9 3-(4⁽⁵⁾-imidazolylmethyl)-2-methylbenzaldehyde 
• 218765-82-3 3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-one 
• 218765-83-4 1-(3-Isopropyl-4-methyl-pent-4-enyl)-3-methoxymethoxymethyl-2-methyl-benzene 
• 218765-84-5 [3-(3-Isopropyl-4-methyl-pent-4-enyl)-2-methyl-phenyl]-methanol 
• 218765-80-1 3-Isopropyl-1-(3-methoxymethoxymethyl-2-methyl-phenyl)-4-methyl-pent-4-en-1-ol 
• 146197-52-6 4-(α-hydroxy-3-methoxymethoxymethyl-2-methylbenzyl)-1-triphenylmethylimidazole 

Relevant articles and documents

A formal synthesis of crinipellin B based on the arene-alkene meta- photocycloaddition reaction

Starting from triethyl phosphonopropionate and 3-nitro-2-methylbenzoic acid, a formal synthesis of crinipellin B was achieved. The strategy draws on the use of a novel version of the arene-alkene meta-photocycloaddition reaction that proceeds with the generation of 4 rings and 4 quaternary stereocenters in one synthetic operation.