726842
(R)-(+)-4-甲氧基-α-甲基苄胺
ChiPros®, produced by BASF, 99%
别名:
(R)-(+)-1-(4-甲氧基苯基)乙胺
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C9H13NO
化学文摘社编号:
分子量:
151.21
UNSPSC Code:
12352112
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2413029
产品名称
(R)-(+)-4-甲氧基-α-甲基苄胺, ChiPros®, produced by BASF, 99%
InChI
1S/C9H13NO/c1-7(10)8-3-5-9(11-2)6-4-8/h3-7H,10H2,1-2H3/t7-/m1/s1
SMILES string
COc1ccc(cc1)[C@@H](C)N
InChI key
JTDGKQNNPKXKII-SSDOTTSWSA-N
assay
≥98.5% (GC)
99%
form
liquid
optical purity
enantiomeric excess: ≥98.5%
density
1.024 g/mL at 20 °C (lit.)
functional group
amine
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
(R)-(+)-4-Methoxy-α-methylbenzylamine can be used as a reactant to prepare:
- 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.
Legal Information
ChiPros is a registered trademark of BASF SE
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Synthesis of (+)-and (-)-Geissman-Waiss lactone from chiral sulfonium salts
Lopez-Gonzalez R, et al.
Tetrahedron Letters, 12(24), 151697-151697 (2020)
Improved hemicryptophane hosts for the stereoselective recognition of glucopyranosides
Schmitt A, et al.
Organic & Biomolecular Chemistry, 12(24), 4211-4217 (2014)
Yohan Park et al.
Archives of pharmacal research, 35(8), 1393-1401 (2012-09-04)
Thirty two thiourea derivatives were prepared and their agonistic activities on the retinoic acid receptor-related orphan receptor α (RORα) were evaluated. The replacement of the 3-allyl-2-imino-thiazolidin-4-one moiety of the lead compound CGP52608 (1) with various functional group substituted aromatic rings
商品
Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.
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.
联系客户支持