726656
(S)-(-)-4-甲氧基-α-甲基苄胺
ChiPros®, produced by BASF, 99%
别名:
(S)-(-)-1-(4-甲氧基苯基)乙胺
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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:
3196456
Assay:
≥98.5% (GC), 99%
Form:
liquid
Quality Level
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
SMILES string
COc1ccc(cc1)[C@H](C)N
InChI
1S/C9H13NO/c1-7(10)8-3-5-9(11-2)6-4-8/h3-7H,10H2,1-2H3/t7-/m0/s1
InChI key
JTDGKQNNPKXKII-ZETCQYMHSA-N
Application
(S)-(−)-4-Methoxy-α-methylbenzylamine is employed in the synthesis of S(+)-4-(1-phenylethylamino)quinazolines, as human immunoglobuline E inhibitor and haloaryl-β-amino acids. It is also used as a precursor to prepare chiral intermediate in the total synthesis of solanoeclepin A.
Legal Information
ChiPros is a registered trademark of BASF SE
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signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.
The asymmetric synthesis of β-haloaryl-β-amino acid derivatives.
Bull S D, et al.
Synlett, 2000(09), 1257-1260 (2000)
Novel Synthesis of the ABC Rings of Solanoeclepin A.
Lin Y T, et al.
Organic Letters, 16(22), 5948-5951 (2014)
S (+)-4-(1-phenylethylamino) quinazolines as inhibitors of human immunoglobuline E synthesis: potency is dictated by stereochemistry and atomic point charges at N-1.
Berger M, et al.
Journal of Medicinal Chemistry, 44(18), 3031-3038 (2001)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 726656-25G | 04061832862224 |
| 726656-100G | 04061832862217 |