106800-17-3

Basic information

• Product Name: 3-(2,3,4-TRIMETHOXY-PHENYL)-PROPAN-1-OL
• Synonyms: 3-(2,3,4-TRIMETHOXY-PHENYL)-PROPAN-1-OL
• CAS NO: 106800-17-3
• Molecular Formula: C₁₂H₁₈O₄
• Molecular Weight: 226.26892
• Mol File: 106800-17-3.mol

Chemical Properties

• Boiling Point: 333.137°C at 760 mmHg
• Flash Point: 155.276°C
• Appearance: /
• Density: 1.086g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.507
• CAS DataBase Reference: 3-(2,3,4-TRIMETHOXY-PHENYL)-PROPAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2,3,4-TRIMETHOXY-PHENYL)-PROPAN-1-OL(106800-17-3)
• EPA Substance Registry System: 3-(2,3,4-TRIMETHOXY-PHENYL)-PROPAN-1-OL(106800-17-3)

Safety Data

• Hazardous Substances Data: 106800-17-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3-(2,3,4-Trimethoxy-phenyl)-propan-1-ol is used as a chemical intermediate for the synthesis of various organic compounds, particularly in the development of pharmaceuticals. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications.
Used in Fragrance Production:
In the fragrance industry, 3-(2,3,4-Trimethoxy-phenyl)-propan-1-ol is utilized as a key component in the formulation of various scents. Its aromatic properties contribute to the creation of unique and complex fragrances.
Used in Chemical Research:
3-(2,3,4-Trimethoxy-phenyl)-propan-1-ol serves as a reagent in chemical reactions, facilitating the synthesis of new compounds and aiding in the advancement of chemical research. Its versatility in reactions makes it a valuable tool for scientists exploring novel chemical pathways.
Used in the Study of Pharmacological Properties:
3-(2,3,4-Trimethoxy-phenyl)-propan-1-ol is under investigation for its potential pharmacological properties, with researchers examining its impact on biological systems. This exploration may lead to the discovery of new therapeutic agents and a deeper understanding of the compound's interactions with biological targets.

InChI:InChI=1/C12H18O4/c1-14-10-7-6-9(5-4-8-13)11(15-2)12(10)16-3/h6-7,13H,4-5,8H2,1-3H3

Upstream product

• 33130-04-0 3-(2,3,4-trimethoxy-phenyl)-propionic acid 
• 125872-57-3 3-(2,3,4-trimethoxyphenyl)-2-propen-1-ol 

Downstream Products

• 106800-31-1 3-(4-hydroxy-2,3-dimethoxyphenyl)propanol 
• 106800-30-0 3-(2-hydroxy-3,4-dimethoxyphenyl)propanol 
• 106800-32-2 3-(3-hydroxy-2,4-dimethoxyphenyl)propanol 
• 482375-86-0 3-(2,3,4-trimethoxyphenyl)propyl methane-sulfonate 

Relevant articles and documents

Unsymmetrical cyclic diamine compound

A cyclic diamine compound of formula (1): wherein A is (CH2)n, (CH2)n—CH═CH, CO—(CH2)n or CO—(CH2)n—CH═CH, in which n is a number of 0 to 3; Z represents a formula (2) or (3): in which R1, R2, R4, R5 and R6 are individually a hydrogen atom, alkyl group, alkoxy group, halogen atom or nitro group; R3 is a hydrogen atom, alkyl group, alkoxy group, halogen atom, nitro group, naphthyl group, or phenyl group which may be substituted by 1 to 3 substituents selected from the group consisting of alkyl groups, alkoxy groups, halogen atoms, a nitro group and a phenyl group; and X and Y are individually CH or a nitrogen atom; and m is 1 or 2; an acid-addition salt thereof, or a hydrate thereof, and a medicine containing such a compound.

Hydroxyl-Directed Regioselective Monodemethylation of Polymethoxyarenes

Methoxyl groups ortho to β-hydroxyethyl or γ-hydroxypropyl substituents in polymethoxybenzene derivatives were regioselectively demethylated with sodium thioethoxide in N,N-dimethylformamide.Methoxydihydrobenzofurans or methoxychromans were produced by cyclization of the monodemethylated β-hydroxyethyl or γ-hydroxypropyl derivatives, respectively.