チオ酢酸 S-カリウム
チオ酢酸 S-カリウム 価格
もっと(26)
| メーカー |
製品番号 |
製品説明 |
CAS番号 |
包装 |
価格 |
更新時間 |
購入 |
|
富士フイルム和光純薬株式会社(wako)
|
W01APOOR59966 |
エタンチオ酸カリウム
Potassium ethanethioate |
10387-40-3 |
25g |
￥4800 |
2024-03-01 |
購入 |
|
富士フイルム和光純薬株式会社(wako)
|
W01APOOR59966 |
エタンチオ酸カリウム
Potassium ethanethioate |
10387-40-3 |
100g |
￥14400 |
2024-03-01 |
購入 |
|
東京化成工業
|
T2030 |
チオ酢酸 S-カリウム >97.0%(T)
S-Potassium Thioacetate
>97.0%(T) |
10387-40-3 |
25g |
￥4600 |
2024-03-01 |
購入 |
|
東京化成工業
|
T2030 |
チオ酢酸 S-カリウム >97.0%(T)
S-Potassium Thioacetate
>97.0%(T) |
10387-40-3 |
250g |
￥23700 |
2024-03-01 |
購入 |
|
関東化学株式会社(KANTO)
|
22130-3A |
チオ酢酸カリウム 98%
Potassium thioacetate 98% |
10387-40-3 |
100g |
￥16000 |
2024-03-01 |
購入 |
チオ酢酸 S-カリウム 化学特性,用途語,生産方法
外観
白色～褐色, 結晶性粉末
溶解性
水及びエタノールにやや溶けにくく、アセトンにほとんど溶けない。
用途
有機合成原料、重金属沈殿剤。
使用上の注意
不活性ガス封入。
化学的特性
white to light brown crystalline powder, crystals
使用
Potassium Thioacetate is the potassium salt of Thioacetic Acid, a commonly used reagent in organic synthesis for the introduction of thiol groups in molecules.
主な応用
Potassium thioacetate is an organosulfur compound and a salt with the formula CH3COS−K+. This white, water-soluble solid is used as a reagent for preparing thioacetate esters and other derivatives . It acts as a sulfur source in the synthesis of sulfur-containing organic compounds for the synthesis of heterocycles, polymers, transition-metal ligands, nanoparticles, bioactive compounds and macromolecular inclusion complexes. It is also used for palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives and it is also used as a reagent in the conversion of halides to thiols.
反応性
Thioacetate is also a class of sulfur-containing nucleophiles, of which potassium thioacetate is the most widely used reagent. Potassium thioacetate reacts with organic halides to form thioesters, which are often used as thiol-protecting groups.In the classical reaction, potassium thioacetate replaces the bromine atom to form a thiol in which the thioester formed in the first step is subjected to a nucleophilic addition elimination reaction to obtain a thiol via hydrolysis, alcoholysis or ammonolysis. Unlike the thiol formation from bromine and thiourea, this method is not strictly limited to polystyrenes. It can also be extended to poly(meth)acrylate systems. It is important that there is no observation of ester hydrolysis during the process.
チオ酢酸 S-カリウム 上流と下流の製品情報
原材料
準備製品
チオ酢酸 S-カリウム 生産企業
Global( 406)Suppliers
チオ酢酸 S-カリウム スペクトルデータ(1HNMR、IR1、IR2、Raman)
10387-40-3(チオ酢酸 S-カリウム)キーワード:
- 10387-40-3
- Potassium Thioacetic
- Potassium thioacete
- Acetic acid, thio-, potassium salt
- Potassium thioethanoate
- Potassium thioacetate,98%
- Potasium thioacetate
- Potassium thioacetat
- PotassiuM thioacetate, 98% 25GR
- PotassiuM thioacetate, 98% 5GR
- potassium 2-thioxoacetate
- MERCAPTOACETIC ACID, POTASSIUM SALT
- KTAA
- Ethanethioic acid potassium salt
- Ethanethioic acid potassium salt, Thioacetic acid potassium salt, Thiolacetic acid potassium salt
- THIOACETIC ACID S-POTASSIUM SALT
- THIOACETIC ACID POTASSIUM
- THIOACETIC ACID POTASSIUM SALT
- thiolacetic acid potassium salt
- TIOACETIC ACID POTASSIUM SALT
- POTASSIUM THIOLACETATE
- POTASSIUM THIOACETATE
- POTASSIUM THIOACETIC ACID
- S-POTASSIUM THIOACETATE
- Potassium thioacetate/Thioacetic acid potassium salt
- Potassium thioacetate ISO 9001：2015 REACH
- Kaliumthioacetat
- Potassium thioaccetate
- MeCOSK
- Potassium ethanethioate
- Potassium thioactate
- チオ酢酸 S-カリウム
- チオ酢酸カリウム
- チオ酢酸カリウム塩
- カリウム チオ酢酸
- チオ酢酸 S‐カリウム
- エタンチオ酸カリウム