推荐产品
等級
produced by BASF
化驗
≥98.5% (GC)
99%
形狀
liquid
光學純度
enantiomeric excess: ≥98.5%
密度
1.024 g/mL at 20 °C (lit.)
SMILES 字串
COc1ccc(cc1)[C@@H](C)N
InChI
1S/C9H13NO/c1-7(10)8-3-5-9(11-2)6-4-8/h3-7H,10H2,1-2H3/t7-/m1/s1
InChI 密鑰
JTDGKQNNPKXKII-SSDOTTSWSA-N
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應用
- Enantiopure stereoisomers of hemicryptophanes, which are used for the recognition of glucopyranosides.
- Bicyclic Geissman-Waiss lactone via intramolecular ring-closure reaction of the diastereomeric mixture of sulfonium salts.
- N-[(1R)-1-(4-Methoxyphenyl)ethyl]-N′-methylthiourea by reacting with methyl isothiocyanate.
法律資訊
訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
商品
Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.
Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.
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