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化驗
99%
光學活性
[α]20/D −152.4°, c = 2 in acetone
光學純度
ee: 98% (GLC)
mp
97-99 °C (lit.)
SMILES 字串
CC(=O)O[C@@H](C(O)=O)c1ccccc1
InChI
1S/C10H10O4/c1-7(11)14-9(10(12)13)8-5-3-2-4-6-8/h2-6,9H,1H3,(H,12,13)/t9-/m1/s1
InChI 密鑰
OBCUSTCTKLTMBX-SECBINFHSA-N
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一般說明
(R)- 和 (S)-异构体可作为手性衍生剂用于 α-氘化羧酸、醇和胺对映体纯度的核磁共振检测。
應用
(R)-(-)-O-Acetylmandelic acid may be used as a precursor to prepare a chiral diamine, which is an intermediate to prepare Utenone A. It may also be used to prepare ethyl (2′R)-2′-acetoxy-2′-phenylethanoate.
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
Eyeshields, Gloves, type N95 (US)
Modular ligand variation in calcium bisimidazoline complexes: effects on ligand redistribution and hydroamination catalysis.
Dalton Transactions, 40(30), 7693-7696 (2011)
Chiroptical features and luminescence behaviour of macrocyclic tetra (4-quinolyl)-complexes: surprising absence of exciton coupling.
J. Chem. Soc. Perkin Trans. II, 11, 2415-2418 (1999)
An efficient synthesis of chiral nonracemic diamines: application in asymmetric synthesis.
Tetrahedron Letters, 39(1), 167-170 (1998)
Tritiated chiral alkanes as substrates for soluble methane monooxygenase from Methylococcus capsulatus (Bath): probes for the mechanism of hydroxylation.
Journal of the American Chemical Society, 119(8), 1818-1827 (1997)
J. Chem. Soc. Perkin Trans. II, 83-83 (1983)
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