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方案
99%
表单
liquid
旋光性
[α]19/D −40°, neat
光学纯度
ee: ≥97% (HPLC)
折射率
n20/D 1.563 (lit.)
沸点
171 °C/15 mmHg (lit.)
密度
1.01 g/mL at 25 °C (lit.)
官能团
amine
phenyl
SMILES字符串
C[C@H](NCc1ccccc1)c2ccccc2
InChI
1S/C15H17N/c1-13(15-10-6-3-7-11-15)16-12-14-8-4-2-5-9-14/h2-11,13,16H,12H2,1H3/t13-/m0/s1
InChI key
ZYZHMSJNPCYUTB-ZDUSSCGKSA-N
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应用
(S)-(−)-N-Benzyl-α-methylbenzylamine can be used:
- In one of the key synthetic steps for the preparation of a cardioprotective drug named CP-060S.
- To prepare (1S,2S,3S,5R)-tert-butyl 3-[benzyl((S)-1-phenylethyl)amino]-6,6-dimethylbicyclo[3.1.1]heptane-2-carboxylate, an intermediate used to synthesize pinane-based β- and γ-amino acids.
- To prepare urea derivatives as potent antimicrobial agents.
警示用语:
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
历史批次信息供参考:
分析证书(COA)
New urea derivatives as potential antimicrobial agents: Synthesis, biological evaluation, and molecular docking studies
Antibiotics, 8(4), 178-178 (2019)
Stereoselective synthesis of pinane-based beta-and gamma-amino acids via conjugate addition of lithium amides and nitromethane
Tetrahedron Asymmetry, 21(20), 2498-2504 (2010)
Practical Synthesis of Novel Cardioprotective Drug, CP-060 S
Organic Process Research & Development, 5(2), 122-126 (2001)
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