28452
Isopropyl cyanoacetate
≥98.0%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
NCCH2COOCH(CH3)2
CAS Number:
Molecular Weight:
127.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
236-421-3
Beilstein/REAXYS Number:
1756014
MDL number:
Assay:
≥98.0%
assay
≥98.0%
refractive index
n20/D 1.416
bp
207 °C (lit.)
density
1.013 g/mL at 20 °C (lit.)
SMILES string
CC(C)OC(=O)CC#N
InChI
1S/C6H9NO2/c1-5(2)9-6(8)3-4-7/h5H,3H2,1-2H3
InChI key
BESQLCCRQYTQQI-UHFFFAOYSA-N
Application
Isopropyl cyanoacetate was used in the synthesis of 3-substituted coumarins by undergoing Knöevenagel reactions with aldehydes and ketones.
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
197.6 °F - closed cup
flash_point_c
92 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Articles
Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.
Use of isopropyl alcohol as a solvent in Ti (O-i-Pr)4 catalyzed Knoevenagel reactions.
Tetrahedron, 61(33), 7981-7985 (2005)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 28452-250ML | 04061836691738 |