Assay
≥95%
form
powder or crystals
reaction suitability
reaction type: Carbonylations
mp
190 °C (dec.) (lit.)
application(s)
peptide synthesis
storage temp.
2-8°C
SMILES string
O=C1CCC(=O)N1OC(=O)ON2C(=O)CCC2=O
InChI
1S/C9H8N2O7/c12-5-1-2-6(13)10(5)17-9(16)18-11-7(14)3-4-8(11)15/h1-4H2
InChI key
PFYXSUNOLOJMDX-UHFFFAOYSA-N
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General description
Application
- As an activating reagent for the reactive patterning of polymer brushes to couple primary amines via post-functionalization.
- As an alkoxycarbonylating reagent for a variety of primary and sterically hindered secondary alcohols, which further allows the synthesis of different structurally diverse carbamates.
- As a coupling agent for the synthesis of thiophospholipids, commonly used for anchoring biomembranes to gold surfaces.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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