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重要文件

726656

Sigma-Aldrich

(S)-(-)-4-甲氧基-α-甲基苄胺

ChiPros®, produced by BASF, 99%

同義詞:

(S)-(-)-1-(4-甲氧基苯基)乙胺

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About This Item

經驗公式(希爾表示法):
C9H13NO
CAS號碼:
分子量::
151.21
Beilstein:
3196456
MDL號碼:
分類程式碼代碼:
12352112
PubChem物質ID:
NACRES:
NA.22

等級

produced by BASF

化驗

≥98.5% (GC)
99%

形狀

liquid

光學純度

enantiomeric excess: ≥98.5%

密度

1.024 g/mL at 20 °C (lit.)

官能基

amine

SMILES 字串

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 密鑰

JTDGKQNNPKXKII-ZETCQYMHSA-N

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應用

(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.

法律資訊

ChiPros is a registered trademark of BASF SE

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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分析證明 (COA)

Lot/Batch Number

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存取文件庫

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)
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)

文章

ChiPros Chiral Amines

Chiral amines play an important role in stereoselective organic synthesis. They are used directly as resolving agents, building blocks, or chiral auxiliaries.

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