ALD00615
Ethyl (S,E)-2-((mesitylsulfinyl)imino)acetate
≥95%
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About This Item
Empirical Formula (Hill Notation):
C13H17NO3S
CAS Number:
Molecular Weight:
267.34
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.22
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Quality Level
Assay
≥95%
form
powder
reaction suitability
reaction type: C-C Bond Formation
storage temp.
−20°C
SMILES string
[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
Application
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.
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Product No.
Description
Pricing
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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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
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