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(S)-(-)-1-Phenylethylamine - 10mM in DMSO, high purity , CAS No.2627-86-3
Basic Description
Synonyms
2627-86-3 | (S)-(-)-1-Phenylethylamine | (1S)-1-phenylethanamine | (S)-1-phenylethanamine | (S)-(-)-alpha-Methylbenzylamine | (S)-1-Phenylethylamine | L-1-Phenylethylamine | L-alpha-Methylbenzylamine | L(-)-alpha-Methylbenzylamine | (S)-alpha-Methylbenzenemethanamine | (s)-(
Specifications & Purity
10mM in DMSO
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Used in a one-pot, multi-component synthesis of a highly substituted, chiral pyrrole
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic nitrogen compounds
Class
Organonitrogen compounds
Subclass
Amines
Intermediate Tree Nodes
Not available
Direct Parent
Aralkylamines
Alternative Parents
Benzene and substituted derivatives Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Aralkylamine - Benzenoid - Monocyclic benzene moiety - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as aralkylamines. These are alkylamines in which the alkyl group is substituted at one carbon atom by an aromatic hydrocarbyl group.
External Descriptors
1-phenylethylamine
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
(1S)-1-phenylethanamine
INCHI
InChI=1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3/t7-/m0/s1
InChIKey
RQEUFEKYXDPUSK-ZETCQYMHSA-N
Smiles
CC(C1=CC=CC=C1)N
Isomeric SMILES
C[C@@H](C1=CC=CC=C1)N
WGK Germany
1
RTECS
DP5775000
UN Number
2922
Molecular Weight
121.18
Beilstein
2204907
Reaxy-Rn
636127
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636127&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Air and moisture sensitive
Refractive Index
1.526
Specific Rotation[α]
-39 ° (neat)
Flash Point(°F)
158 °F
Flash Point(°C)
70 °C
Boil Point(°C)
187°C
Melt Point(°C)
-10°C
Molecular Weight
121.180 g/mol
XLogP3
1.200
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
1
Exact Mass
121.089 Da
Monoisotopic Mass
121.089 Da
Topological Polar Surface Area
26.000 Ų
Heavy Atom Count
9
Formal Charge
0
Complexity
74.600
Isotope Atom Count
0
Defined Atom Stereocenter Count
1
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Qian Wang, Limei Sheng, Xuan Guo, Rong Chen, Chengjie Zhou, Fu Yang.
(2023)
Functionalized poly(ionic liquid)s bridging Pd NPs and lipase for highly efficient dynamic kinetic resolution of chiral amine. APPLIED CATALYSIS A-GENERAL,
666
(119426).
2.
Bing Tang, Shixun Wang, Haochen Liu, Nanli Mou, Arsenii S. Portniagin, Peigang Chen, Ye Wu, Xiaoqing Gao, Dangyuan Lei, Andrey L. Rogach.
(2023)
Chiral Ligand-Induced Inversion and Tuning of Excitonic Optical Activity in Intrinsically Chiral CsPbBr3 Perovskite Nanoplatelets. Advanced Optical Materials,
(2301524).
3.
Zhangchuan Wen, Rong Lu, Fan Gu, Kai Zheng, Lijie Zhang, Huile Jin, Yihuang Chen, Shun Wang, Shuang Pan.
(2022)
Enabling Efficient Blue-Emissive Circularly Polarized Luminescence by In Situ Crafting of Chiral Quasi-2D Perovskite Nanosheets within Polymer Nanofibers. ADVANCED FUNCTIONAL MATERIALS,
33
(7):
(2212095).
4.
Datong Wu, Cong Ma, Ting Wan, Pengfen Zhu, Yong Kong.
(2022)
Strategies to synthesize a chiral helical polymer accompanying with two stereogenic centers for chiral electroanalysis. ANALYTICA CHIMICA ACTA,
1206
(339810).
5.
Xu Zhu, Ruiying Wang, Yafang Ge, Yingling Dong, Benlai Wu.
(2022)
A new two-dimensional homochiral cadmium(II) coordination polymer: synthesis, structure determination, optical properties, and fluorescent sensing. JOURNAL OF COORDINATION CHEMISTRY,
6.
Youming Huang, Hongyi Chen, Wenting Zheng, Qingle Zeng.
(2020)
Cu2O-catalyzed C–S coupling of quaternary ammonium salts and sodium alkane-/arene-sulfinates. TETRAHEDRON LETTERS,
61
(152320).
7.
Lei Shi,Yizhan Wang,Bao Li,Lixin Wu.
(2014-05-09)
Polyoxometalate complexes for oxidative kinetic resolution of secondary alcohols: unique effects of chiral environment, immobilization and aggregation.. Dalton transactions (Cambridge, England : 2003),
43
((24)):
(9177-9188).
8.
Yuan Wang, Mu-Sen Song, Jiaqi Zhao, Zhen Li, Tinglei Wang, Hai Wang, Hai-Yu Wang, Yu Wang.
(2024)
Chiral Perovskite Heterostructure Films of CsPbBr3 Quantum Dots and 2D Chiral Perovskite with Circularly Polarized Luminescence Performance and Energy Transfer. ACS Nano,
18
(33):
(22334-22343).
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8 Citations