Skip to Content
Merck
All Photos(2)

Documents

ALD00616

Sigma-Aldrich

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

≥95%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C13H17NO3S
CAS Number:
Molecular Weight:
267.34
NACRES:
NA.22

Quality Level

Assay

≥95%

form

powder

reaction suitability

reaction type: C-C Bond Formation

mp

62-65 °C

storage temp.

−20°C

Application

Ethyl (R,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.

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service