跳转至内容
Merck
CN

335614

Sigma-Aldrich

3-氯苯丙酮

98%

别名:

β-氯苯丙酮, 3-氯-1-苯基-1-丙酮

登录查看公司和协议定价


About This Item

线性分子式:
ClCH2CH2COC6H5
CAS号:
分子量:
168.62
Beilstein:
2043580
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

表单

solid

沸点

113-115 °C/4 mmHg (lit.)

mp

48-50 °C (lit.)

官能团

chloro
ketone
phenyl

SMILES字符串

ClCCC(=O)c1ccccc1

InChI

1S/C9H9ClO/c10-7-6-9(11)8-4-2-1-3-5-8/h1-5H,6-7H2

InChI key

KTJRGPZVSKWRTJ-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

应用

3-氯苯丙酮可用于使用固定在藻酸钙凝胶珠中的预热的 产朊假丝酵母 细胞,对(S)-3-氯-1-苯基丙醇进行不对称还原。 利用衍生自(S)-α,α-二苯基脯氨醇的 原位 生成的恶唑硼烷催化剂,它也可通过不对称还原用于合成(R)-3-氯-1-苯基-1-丙醇。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Asymmetric Synthesis of (R)-Fluoxetine: A Practical Approach Using Recyclable and in-situ Generated Oxazaborolidine Catalyst.
Padiya K, et al.
Chin. J. Chem., 27(6), 1137-1140 (2009)
Yang Gen-Sheng et al.
Biotechnology letters, 31(12), 1879-1883 (2009-07-28)
An efficient method for asymmetric reduction of (S)-3-chloro-1-phenylpropanol from 3-chloropropiophenone was developed using preheated Candida utilis cells immobilized in calcium alginate gel beads. Heating the immobilized cells (bead diameter 1.5 mm) at 45 degrees C for 50 min allowed the
Milada Šírová et al.
Journal of drug targeting, 25(9-10), 796-808 (2017-07-21)
Polymer carriers based on N-(2-hydroxypropyl)methacrylamide (HPMA) copolymers with incorporated organic nitrates as nitric oxide (NO) donors were designed with the aim to localise NO generation in solid tumours, thus highly increasing the enhanced permeability and retention (EPR) effect. The NO
Yu-Chang Liu et al.
Organic & biomolecular chemistry, 13(7), 2146-2152 (2014-12-23)
Styrene monooxygenase (SMO) can catalyze the kinetic resolution of secondary allylic alcohols to provide enantiopure glycidol derivatives. To overcome the low theoretical yield of kinetic resolution, we designed a one-pot two-step enzymatic cascade using prochiral α,β-unsaturated ketones as the substrates.

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.

联系技术服务部门