118943-21-8

Basic information

• Product Name: 3-(4-METHOXYPHENOXY)-1-PROPANOL 98
• Synonyms: 3-(4-METHOXYPHENOXY)-1-PROPANOL 98;3-(4-methoxyphenoxy)-1-propanol
• CAS NO: 118943-21-8
• Molecular Formula: C₁₀H₁₄O₃
• Molecular Weight: 182.22
• Mol File: 118943-21-8.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 301.4°C at 760 mmHg
• Flash Point: 136.1°C
• Appearance: /
• Density: 1.084g/cm³
• Vapor Pressure: 0.000469mmHg at 25°C
• Refractive Index: 1.512
• PKA: 14.78±0.10(Predicted)
• CAS DataBase Reference: 3-(4-METHOXYPHENOXY)-1-PROPANOL 98(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-METHOXYPHENOXY)-1-PROPANOL 98(118943-21-8)
• EPA Substance Registry System: 3-(4-METHOXYPHENOXY)-1-PROPANOL 98(118943-21-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 118943-21-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H14O3/c1-12-9-3-5-10(6-4-9)13-8-2-7-11/h3-6,11H,2,7-8H2,1H3

Upstream product

• 150-76-5 4-methoxy-phenol 
• 627-30-5 1-chloro-3-hydroxypropane 
• 1141498-03-4 1-[3-(3-methylbut-3-enyloxy)propoxy]-4-methoxybenzene 
• 627-18-9 1-bromo-3-propanol 
• 1141498-12-5 1-[3-(4-iodo-3-methoxy-3-methylbutoxy)propoxy]-4-methoxybenzene 

Downstream Products

• 6267-37-4 1-(3-bromopropoxy)-4-methoxybenzene 
• 958356-62-2 2-[3-(4-Methoxy-phenoxy)-propoxy]-3H-pyrido[2,3-d]pyrimidin-4-one 
• 1335100-08-7 3-(2,5-bis(chloromethyl)-4-methoxyphenoxy)propan-1-ol 
• 1335100-12-3 C₁₄H₁₅N₂O₅S^(1-)*Na⁽¹⁺⁾ 
• 1335100-09-8 C₁₄H₁₆N₂O₃ 
• 1335100-10-1 C₁₅H₁₈N₂O₅S 
• 1335100-11-2 C₁₄H₁₅IN₂O₂ 
• 1374019-07-4 (E)-5-(4-methoxyphenoxy)pent-2-enoic acid 
• 1361383-48-3 (E)-5-(4-methoxyphenoxy)pent-2-enoyl chloride 
• 1361383-49-4 methyl 2-isopentyl-6-(2-(4-methoxyphenoxy)ethyl)-4-oxo-5,6-dihydropyran-3-carboxylate 
• 1361397-15-0 C₂₁H₂₈O₆ 
• 1374019-06-3 ethyl (E)-5-(4-methoxyphenoxy)pent-2-enoate 

Relevant articles and documents

Design, synthesis, and biological evaluation of new growth inhibitors of Trypanosoma cruzi (epimastigotes)

As a continuation of our project aimed at the search for new chemotherapeutic agents against Chagas' disease, several drugs structurally related to the insect growth regulator Fenoxycarb and the naturally occurring juvenfie hormone of insects were designed, synthesized, and evaluated as antiproliferative agents against the parasite responsible of this disease. Isoprenoid derivatives (compounds 33, 34, 36, and 37) were potent growth inhibitors of Trypanosoma cruzi epimastigotes. In addition, taking into account the high activity observed for compound 30 and the inhibitory action of related compounds, the allyl ether moiety bonded at the polar extreme of these inhibitors proved to be a promising group for the design of new drugs.

GLYCOSIDE COMPOUND AND PREPARATION METHOD THEREFOR, COMPOSITION, APPLICATION, AND INTERMEDIATE

The present invention discloses a glycoside compound represented by Formula III, and a preparation method, a composition, use and an intermediate thereof. The glycoside compound provided in the present invention has simple preparation method, can significantly increase the expression of VEGF-A mRNA, and is effective in promoting the angiogenesis. This provides a reliable guarantee for the development of drugs with pro-angiogenic activity for treating cerebral infarction cerebral stroke, myocardial infarction, and ischemic microcirculatory disturbance of lower limbs.

Total synthesis of mevashuntin

The total synthesis of (±)-mevashuntin, a structurally unique naturally occurring pyrano-naphthoquinone-thiazolone, is described. The route is centered upon a late stage regioselective Diels-Alder reaction between two highly functionalized components, as