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化驗
98%
光學活性
[α]21/D −80°, c = 0.85 in ethanol
反應適用性
reaction type: solution phase peptide synthesis
bp
87-90 °C (lit.)
應用
peptide synthesis
SMILES 字串
OC[C@H](NCc1ccccc1)c2ccccc2
InChI
1S/C15H17NO/c17-12-15(14-9-5-2-6-10-14)16-11-13-7-3-1-4-8-13/h1-10,15-17H,11-12H2/t15-/m0/s1
InChI 密鑰
FTFBWZQHBTVPEO-HNNXBMFYSA-N
應用
用于不对称合成 α-氨基膦酸。制取光学纯 β-取代胺的实用工艺路线所需原料。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Tetrahedron Letters, 35, 7223-7223 (1994)
The Journal of organic chemistry, 61(11), 3687-3693 (1996-05-31)
A simple and general asymmetric synthesis of alpha-amino phosphonic acids is described. The method involves the highly selective addition of trialkyl phosphite onto various chiral oxazolidines. Oxazaphosphorinanes thus obtained with an excellent diastereoselectivity furnish the corresponding (S)-alpha-substituted amino phosphonic acids
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