Search Thermo Fisher Scientific
元素の検索
構造の検索Thermo Scientific Chemicals
2-Thiophenemethylamine, 94%, Thermo Scientific Chemicals
製品番号（カタログ番号）： A11700.22
100 g, Each
化学物質識別子
CAS
27757-85-3
IUPAC Name
(thiophen-2-yl)methanaminium
Molecular Formula
C5H8NS
InChI Key
FKKJJPMGAWGYPN-UHFFFAOYSA-O
SMILES
[NH3+]CC1=CC=CS1
仕様
スペックシートAppearance (Color)
Clear colorless to yellow
Form
Liquid
Assay (GC)
≥92.0%
Refractive Index
1.5645-1.5695 @ 20°C
概要
2-Thiophenemethylamine is Reactant involved in synthesis of: Triazole-linked-thiopene conjugates. It is used for biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein.It is a reactant involved in studies of organocatalyzed asymmetric reductive amination of ketones.
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
2-Thiophenemethylamine is Reactant involved in synthesis of: Triazole-linked-thiopene conjugates. It is used for biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein.It is a reactant involved in studies of organocatalyzed asymmetric reductive amination of ketones.
Solubility
Easily soluble in ethanol and Chloroform.
Notes
Air Sensitive. Store under dry inert gas. Store away from air.
2-Thiophenemethylamine is Reactant involved in synthesis of: Triazole-linked-thiopene conjugates. It is used for biomimetic model for studies of metal detoxification and oxidative stress involving metallothionein.It is a reactant involved in studies of organocatalyzed asymmetric reductive amination of ketones.
Solubility
Easily soluble in ethanol and Chloroform.
Notes
Air Sensitive. Store under dry inert gas. Store away from air.
RUO – Research Use Only
図
ドキュメントおよびダウンロード
証明書
ロット番号または部分ロット番号で検索
よくあるご質問（FAQ）
引用および参考文献
Search citations by name, author, journal title or abstract text