The Ethane, (methylthio)-, with CAS registry number 624-89-5, belongs to the following product categories: (1)Organic Building Blocks; (2)Sulfides/Disulfides; (3)Sulfur Compounds. It has the systematic name of (methylsulfanyl)ethane. This chemical is a kind of clear colorless liquid. The main use of this chemical is organic synthesis.

Physical properties of Ethane, (methylthio)-L: (1)ACD/LogP: 1.42; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.42; (4)ACD/LogD (pH 7.4): 1.42; (5)ACD/BCF (pH 5.5): 7.05; (6)ACD/BCF (pH 7.4): 7.05; (7)ACD/KOC (pH 5.5): 140.85; (8)ACD/KOC (pH 7.4): 140.85; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 25.3 Å²; (13)Index of Refraction: 1.433; (14)Molar Refractivity: 23.94 cm³; (15)Molar Volume: 92 cm³; (16)Polarizability: 9.49×10^-24cm³; (17)Surface Tension: 23.2 dyne/cm; (18)Enthalpy of Vaporization: 29.53 kJ/mol; (19)Vapour Pressure: 186 mmHg at 25°C.

Preparation: this chemical can be prepared by iodomethane and ethanethiol. This reaction will need reagents KOH, DMSO. The reaction time is 2 hour(s). The yield is about 88%.

Uses of p-Chloropropiophenone: it can be used to produce methanesulfinyl-ethane. This reaction will need reagents 35percent aq. H₂O₂ and solvent methanol. The reaction time is 2 hour(s). The yield is about 50%.

When you are using this chemical, please be cautious about it as the following:
The Ethane, (methylthio)- is highly flammable, so keep it away from sources of ignition. When use this chemical, do not breathe vapour and avoid contact with skin and eyes.

You can still convert the following datas into molecular structure:
(1)SMILES: S(CC)C
(2)InChI: InChI=1/C3H8S/c1-3-4-2/h3H2,1-2H3
(3)InChIKey: WXEHBUMAEPOYKP-UHFFFAOYAC
(4)Std. InChI: InChI=1S/C3H8S/c1-3-4-2/h3H2,1-2H3
(5)Std. InChIKey: WXEHBUMAEPOYKP-UHFFFAOYSA-N