Names | |
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Preferred IUPAC name 3-Methylthiophene | |
Other names 3-Thiotolene | |
Identifiers | |
3D model (JSmol) | |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.009.530 |
EC Number |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
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Properties | |
C5H6S | |
Molar mass | 98.16 g·mol−1 |
Appearance | colorless liquid |
Density | 1.016 g/cm3 |
Melting point | −69 °C (−92 °F; 204 K) |
Boiling point | 114 °C (237 °F; 387 K) |
0.4 g/l | |
Hazards | |
GHS pictograms | |
GHS Signal word | Danger |
H225, H302, H312, H315, H319, H332, H335 | |
P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+312, P302+352, P303+361+353, P304+312, P304+340, P305+351+338, P312, P321, P322, P330, P332+313, P337+313, P362, P363 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
3-Methylthiophene is an organosulfur compound with the formula CH3C4H3S. It is a colorless, flammable liquid. It can be produced by sulfidation of 2-methylsuccinate. [1]
In mathematics, the derivative of a function of a real variable measures the sensitivity to change of the function value with respect to a change in its argument. Derivatives are a fundamental tool of calculus. For example, the derivative of the position of a moving object with respect to time is the object's velocity: this measures how quickly the position of the object changes when time advances.
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2-Methylthiophene is an organosulfur compound with the formula CH3C4H3S. It is a colorless, flammable liquid. It can be produced by Wolff-Kishner reduction of thiophene-2-carboxaldehyde.
2-Methylsuccinic acid is an organic compound with the formula HO2CCH(CH3)CH2CO2H. A white solid, it is the simplest chiral dicarboxylic acid. It is a recurring component of urban aerosols. Salts and esters of 2-methylsuccinic acid are called 2-methylsuccinates.
Methylthiophene may refer to: