跳转至内容
Merck

ALD00615

Sigma-Aldrich

Ethyl (S,E)-2-((mesitylsulfinyl)imino)acetate

≥95%

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C13H17NO3S
分子量:
267.34
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.22

质量水平

方案

≥95%

表单

powder

反应适用性

reaction type: C-C Bond Formation

储存温度

−20°C

SMILES字符串

[S](=O)(\N=C\C(=O)OCC)c1c(cc(cc1C)C)C

InChI

1S/C13H17NO3S/c1-5-17-12(15)8-14-18(16)13-10(3)6-9(2)7-11(13)4/h6-8H,5H2,1-4H3/b14-8+

InChI key

OUMNTVUUJPMNPJ-RIYZIHGNSA-N

应用

Ethyl (S,E)-2-((mesitylsulfinyl)imino)acetate is a chiral glyoxylate-derived sulfinimine reagent used for the synthesis of optically pure amino acids through a decarboxylative radical cross-coupling reaction.

相关产品

产品编号
说明
价格

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助,请联系 客户支持

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

Shengyang Ni et al.
Angewandte Chemie (International ed. in English), 57(44), 14560-14565 (2018-09-14)
The direct union of primary, secondary, and tertiary carboxylic acids with a chiral glyoxylate-derived sulfinimine provides rapid access into a variety of enantiomerically pure α-amino acids (>85 examples). Characterized by operational simplicity, this radical-based reaction enables the modular assembly of

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