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Thermo Scientific Chemicals
4-Methoxybenzyl mercaptan, 98%
CAS: 6258-60-2 | C8H10OS | 154.23 g/mol
化学物質識別子
CAS6258-60-2
IUPAC Name(4-methoxyphenyl)methanethiol
Molecular FormulaC8H10OS
InChI KeyPTDVPWWJRCOIIO-UHFFFAOYSA-N
SMILESCOC1=CC=C(CS)C=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless to pale yellow
Assay (GC)≥95.0%
CommentSpecification differs for U.S. and non-U.S. material where indicated
Identification (FTIR)Conforms (non-U.S. specification)
Refractive Index1.5735-1.5775 @ 20°C
さらに表示
4-Methoxybenzyl mercaptan is used to synthesize many ω-mercapto amino acids with side-chain lengths ranging from 3-5 methylene units. It is used as an internal standard in the Quantitative determination of wine polyfunctional mercaptans at the level of nanogram per liter.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-Methoxybenzyl mercaptan is used to synthesize many ω-mercapto amino acids with side-chain lengths ranging from 3-5 methylene units. It is used as an internal standard in the Quantitative determination of wine polyfunctional mercaptans at the level of nanogram per liter.
Solubility
Not miscible or difficult to mix in water.
Notes
Air sensitive. Store under inert gas. Incompatible with oxidizing agents, acids, bases, air.
4-Methoxybenzyl mercaptan is used to synthesize many ω-mercapto amino acids with side-chain lengths ranging from 3-5 methylene units. It is used as an internal standard in the Quantitative determination of wine polyfunctional mercaptans at the level of nanogram per liter.
Solubility
Not miscible or difficult to mix in water.
Notes
Air sensitive. Store under inert gas. Incompatible with oxidizing agents, acids, bases, air.
RUO – Research Use Only
General References:
- Ming Li; Priyadarsi De; Sudershan R. Gondi and Brent S. Sumerlin. End group transformations of RAFT-generated polymers with bismaleimides: Functional telechelics and modular block copolymers. Journal of Polymer Science Part A: Polymer Chemistry. 2008, 46 (15), 5093-5100.
- Howard E. Katz; Jerainne Johnson; Andrew J. Lovinger and Wenjie Li. Naphthalenetetracarboxylic Diimide-Based n-Channel Transistor Semiconductors: Structural Variation and Thiol-Enhanced Gold Contacts. J. Am. Chem. Soc. 2000, 122 (32), 7787-7792.