59209-70-0

Basic information

• Product Name: 3-(4-METHYLSULFANYL-PHENYL)-PROPAN-1-OL
• Synonyms: 3-(4-METHYLSULFANYL-PHENYL)-PROPAN-1-OL
• CAS NO: 59209-70-0
• Molecular Formula: C₁₀H₁₄OS
• Molecular Weight: 182.28256
• Mol File: 59209-70-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 314.7°C at 760 mmHg
• Flash Point: 153.3°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 0.000195mmHg at 25°C
• Refractive Index: 1.57
• CAS DataBase Reference: 3-(4-METHYLSULFANYL-PHENYL)-PROPAN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-METHYLSULFANYL-PHENYL)-PROPAN-1-OL(59209-70-0)
• EPA Substance Registry System: 3-(4-METHYLSULFANYL-PHENYL)-PROPAN-1-OL(59209-70-0)

Safety Data

• Hazardous Substances Data: 59209-70-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H14OS/c1-12-10-6-4-9(5-7-10)3-2-8-11/h4-7,11H,2-3,8H2,1H3

Upstream product

• 102016-58-0 p-(methylthio)cinnamic acid 
• 3446-89-7 4-(Methylthio)benzaldehyde 
• 123392-44-9 methyl 3-[4-(methylthio)phenyl]propanoate 

Downstream Products

• 651310-29-1 3-[4-(methylsulfonyl)phenyl]propan-1-ol 
• 116174-33-5 4-(4-methylsulfanyl-phenyl)butyric acid 
• 1057678-77-9 (4-(3-bromopropyl)phenyl)(methyl)sulfane 

Relevant articles and documents

Method used for reduction of tertiary amide into alcohols and/or amines

The invention discloses a method used for reduction of tertiary amide into alcohols and/or amines. The method comprises following steps: tertiary amide, an alkali metal reagent, and a proton donor agent are added into an organic solvent for a following reaction selectively: when the proton donor agent is a raw material alcohol and/or inorganic salt aqueous solution, the reaction product is an alcohol compound and/or tertiary amine compound. The method is capable of realizing selective reduction of tertiary amide into alcohols and tertiary amine compounds, the yield is high, the suitable rangeis wide, operation is safe and simple, the adopted raw materials are cheap and easily available; no precious metal catalyst, toxic silanes, and flammable and combustible metal hydrides are adopted; notoxic by product is generated; reaction is more friendly to the environment; problems in the prior art that amide compound reducing method operation is complex, conditions are strict, and control ofproducts is difficult are solved.

NOVEL PYRAZINE AMIDE COMPOUNDS

The present invention relates to compounds of formula 1 or pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R5, R6 and X- have one of the meanings as indicated in the specification, to their use as a medicament, to their use in the treatment of a disease selected from among respiratory diseases or complaints and allergic diseases of the airways, to pharmaceutical composition comprising at least one of said compound or a pharmaceutically acceptable salt thereof, as well as to medicament combinations containing one or more of said compounds or a pharmaceutically acceptable salt thereof.

Evaluation of the efficiency of the photocatalytic one-electron oxidation reaction of aromatic compounds adsorbed on a TiO2 surface

The TiO2 photocatalytic one-electron oxidation mechanism of aromatic sulfides with a methylene bridging group (-(CH2) n-, n = 0-4) between the 4-(methylthio)phenyl chromophore and the carboxylate binding group on the surfa