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线性分子式:
C6H5CH(CH3)NHCH2C6H5
化学文摘社编号:
分子量:
211.30
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3650264
产品名称
(S)-(-)-N-苄基-α-甲基苄胺, 99%
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
SMILES string
C[C@H](NCc1ccccc1)c2ccccc2
InChI key
ZYZHMSJNPCYUTB-ZDUSSCGKSA-N
assay
99%
form
liquid
optical activity
[α]19/D −40°, neat
optical purity
ee: ≥97% (HPLC)
refractive index
n20/D 1.563 (lit.)
bp
171 °C/15 mmHg (lit.)
density
1.01 g/mL at 25 °C (lit.)
functional group
amine
phenyl
Quality Level
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Application
(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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
New urea derivatives as potential antimicrobial agents: Synthesis, biological evaluation, and molecular docking studies
Patil M, et al.
Antibiotics, 8(4), 178-178 (2019)
Stereoselective synthesis of pinane-based beta-and gamma-amino acids via conjugate addition of lithium amides and nitromethane
Szakonyi Z, et al.
Tetrahedron Asymmetry, 21(20), 2498-2504 (2010)
Practical Synthesis of Novel Cardioprotective Drug, CP-060 S
Kato T, et al.
Organic Process Research & Development, 5(2), 122-126 (2001)
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