761052
1H-Imidazole-1-carboxylic acid-3-butenyl ester
97%
Synonym(s):
Heller-Sarpong Reagent-Homoallyl
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About This Item
Empirical Formula (Hill Notation):
C8H10N2O2
CAS Number:
Molecular Weight:
166.18
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
liquid
refractive index
n20/D 1.488
density
1.107 g/mL at 25 °C
functional group
allyl
storage temp.
2-8°C
SMILES string
O=C(OCCC=C)N1C=CN=C1
InChI
1S/C8H10N2O2/c1-2-3-6-12-8(11)10-5-4-9-7-10/h2,4-5,7H,1,3,6H2
InChI key
BNGLJMQCDKTXTL-UHFFFAOYSA-N
Application
1H-Imidazole-1-carboxylic acid-3-butenyl ester can be used:
- To prepare bis-naphthyridine derived cyclic mismatch binding ligands (CMBLs) which exhibit DNA repeat binding properties.
- As a reagent in the chemoselective esterification of carboxylic acids.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
230.0 °F
Flash Point(C)
110 °C
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
Design and synthesis of cyclic Mismatch-Binding Ligands (CMBLs) with variable linkers by Ring-Closing metathesis and their photophysical and DNA repeat binding properties
Mukherjee S, et al.
Chemistry?A European Journal , 23, 11385-11396 (2017)
Chemoselective esterification and amidation of carboxylic acids with imidazole carbamates and ureas
Heller ST and Sarpong R
Organic Letters, 12(20), 4572-4575 (2010)
Related Content
Professor Heller's research focuses on mild acylation reactions using carbonylimidazole-derived reagents.
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