118943-23-0

Basic information

• Product Name: 3-(4-METHOXYPHENOXY)-1-IODOPROPANE 95
• Synonyms: 3-(4-METHOXYPHENOXY)-1-IODOPROPANE 95
• CAS NO: 118943-23-0
• Molecular Formula: C₁₀H₁₃IO₂
• Molecular Weight: 292.111
• Mol File: 118943-23-0.mol

Chemical Properties

• Melting Point: 21-24 °C(lit.)
• Boiling Point: 330.3°C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.5274 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000322mmHg at 25°C
• Refractive Index: n20/D 1.5758(lit.)
• CAS DataBase Reference: 3-(4-METHOXYPHENOXY)-1-IODOPROPANE 95(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-METHOXYPHENOXY)-1-IODOPROPANE 95(118943-23-0)
• EPA Substance Registry System: 3-(4-METHOXYPHENOXY)-1-IODOPROPANE 95(118943-23-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 118943-23-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-(4-METHOXYPHENOXY)-1-IODOPROPANE 95 is used as a reactant for the preparation of Stigmatellin A (S686780), which is a compound with potential applications in the development of new drugs and therapies. The synthesis of Stigmatellin A is important for exploring its biological properties and potential use in the treatment of various diseases.
Additionally, 1-(3-Iodopropoxy)-4-methoxybenzene, another reactant in the preparation of Stigmatellin A, is also used in the pharmaceutical industry for the same purpose. The development of Stigmatellin A and its derivatives can contribute to the advancement of drug discovery and the creation of novel therapeutic agents.

InChI:InChI=1/C10H13IO2/c1-12-9-3-5-10(6-4-9)13-8-2-7-11/h3-6H,2,7-8H2,1H3

Upstream product

• 150-76-5 4-methoxy-phenol 
• 6267-37-4 1-(3-bromopropoxy)-4-methoxybenzene 
• 20744-03-0 1-(3-chloropropoxy)-4-methoxybenzene 

Downstream Products

• 276690-16-5 (2R,3S,4S,5S)-(-)-1-Benzyloxy-8-(4'-methoxyphenoxy)-3,5-dimethyloctan-2,4-diol 
• 276690-15-4 (2R,3R,5S)-(-)-1-Benzyloxyhydroxy-8-(4'-methoxyphenoxy)-3,5-dimethyloctan-4-one 
• 276690-14-3 (S)-(+)-7-(4'-Methoxyphenoxy)-4-methylheptan-3-one 

Relevant articles and documents

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Diastereo- and enantioselective total synthesis of stigmatellin A

Stigmatellin A (1) isolated from the myxobacterium Stigmatella aurantiaca is a powerful inhibitor of electron transport in mitochondria and chloroplasts. The first highly diastereo- and enantioselective total synthesis of this important natural product is