추천 제품
분석
99%
광학 활성
[α]20/D −152.4°, c = 2 in acetone
광학 순도
ee: 98% (GLC)
mp
97-99 °C (lit.)
SMILES string
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 key
OBCUSTCTKLTMBX-SECBINFHSA-N
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일반 설명
(R)-(-)-O-Acetylmandelic acid is a chiral derivatizing agent for NMR determination of enantiomeric purity of α-deuterated carboxylic acids, alcohols, and amines.
애플리케이션
(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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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)
Modular ligand variation in calcium bisimidazoline complexes: effects on ligand redistribution and hydroamination catalysis.
Dalton Transactions, 40(30), 7693-7696 (2011)
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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