推荐产品
方案
≥95.0% (GC)
旋光性
[α]20/D −20±2°, neat
光学纯度
enantiomeric ratio: ≥99.0:1.0 (GC)
折射率
n20/D 1.520
密度
0.940 g/mL at 20 °C (lit.)
SMILES字符串
CC[C@H](N)c1ccccc1
InChI
1S/C9H13N/c1-2-9(10)8-6-4-3-5-7-8/h3-7,9H,2,10H2,1H3/t9-/m0/s1
InChI key
AQFLVLHRZFLDDV-VIFPVBQESA-N
正在寻找类似产品? 访问 产品对比指南
应用
(S)-(−)-α-Ethylbenzylamine can be used:
- To prepare optically active copolyacrylate polymers with sensing and chiroptical properties.
- As a chiral auxiliary in the preparation of enantioenriched indanone derived α-SCF2H β-keto esters.
警示用语:
Danger
危险声明
危险分类
Acute Tox. 4 Oral - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
170.6 °F
闪点(°C)
77 °C
个人防护装备
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Synthesis and characterization of new optically active poly (acrylamide/methacrylurea-co-vinyl acetate) copolymers with dansyl units
Designed Monomers and Polymers, 18(2), 118-128 (2015)
Asymmetric Electrophilic Difluoromethylthiolation of Indanone-Based β-Keto Esters Using Difluoromethanesulfonyl Hypervalent Iodonium Ylides
Molecules (Basel), 24(2), 221-221 (2019)
商品
手性胺已广泛用于不对称合成,例如用作对映选择性去质子化反应中的手性碱,或用于拆分消旋的酸。
Chiral amines have found widespread application in asymmetric synthesis serving, for instance, as chiral bases in enantioselective deprotonation reactions or being valuable substances for resolving racemic mixtures of acids.
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门