230340
L-(-)-乳酸甲酯
98%, optical purity ee: 97% (GLC)
别名:
(S)-(-)-乳酸甲酯
登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
CH3CH(OH)CO2CH3
化学文摘社编号:
分子量:
104.10
Beilstein:
1720587
EC 号:
MDL编号:
UNSPSC代码:
12352108
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
98%
表单
liquid
旋光性
[α]18/D −8.1°, neat
光学纯度
ee: 97% (GLC)
环保替代产品特性
Safer Solvents and Auxiliaries
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
折射率
n20/D 1.413 (lit.)
沸点
144-145 °C (lit.)
密度
1.09 g/mL at 25 °C (lit.)
官能团
ester
hydroxyl
环保替代产品分类
SMILES字符串
COC(=O)[C@H](C)O
InChI
1S/C4H8O3/c1-3(5)4(6)7-2/h3,5H,1-2H3/t3-/m0/s1
InChI key
LPEKGGXMPWTOCB-VKHMYHEASA-N
正在寻找类似产品? 访问 产品对比指南
一般描述
(-)-L-乳酸甲酯可用作合成包公藤甲素（一种抗青光眼化合物）的手性助剂。
我们致力于为您带来更环保的替代产品，以符合一项或多项绿色化学12项原则。本化合物性质温和，具有生物降解性和水溶性。可作为制备醋酸纤维素(CA)膜的多功能试剂。也可用作多种化合物、聚合物和衍生物生产的中间体。本品已增强为“更安全的溶剂和助剂”。点击此处了解更多信息。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Flam. Liq. 3 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
120.2 °F - closed cup
闪点(°C)
49 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Methyl (S)-lactate as a chiral auxiliary in the asymmetric synthesis of Bao Gong Teng A.
Pham VC and Charlton JL.
The Journal of Organic Chemistry, 60(24), 8051-8055 (1995)
Nicole Borho et al.
Organic & biomolecular chemistry, 1(23), 4351-4358 (2003-12-20)
Chiral recognition and subsequent selective self-organisation into hydrogen-bonded n-mers is observed in supersonic methyl lactate expansions. The nu(OH) and nu(C=O)-vibrations are investigated by ragout-jet FTIR-spectroscopy and lead to the assignment of homo- and heterochiral clusters of at least three different
K Bodenhöfer et al.
Nature, 387(6633), 577-580 (1997-06-05)
Odour perception in humans can sometimes discriminate different enantiomers of a chiral compound, such as limonene. Chiral discrimination represents one of the greatest challenges in attempts to devise selective and sensitive gas sensors. The importance of such discrimination for pharmacology
Zeolite-catalyzed isomerization of triose sugars.
Esben Taarning et al.
ChemSusChem, 2(7), 625-627 (2009-06-30)
Huoming Li et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(38), 11530-11534 (2010-08-31)
RCM + AD = T2: In the presence of the C16-methylene group, regioselective ring-closing metathesis (RCM) formed the (12E)-endocyclic double bond, which underwent Os-catalyzed asymmetric dihydroxylation (AD) to give the desired 12,13-diol intermediate required for the total synthesis of amphidinolide
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持