All Photos(1)
About This Item
Linear Formula:
C6H5CH2OCH2CH2COCH3
CAS Number:
Molecular Weight:
178.23
Beilstein/REAXYS Number:
779045
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
assay
≥97.0%
refractive index
n20/D 1.505
bp
90-92 °C/0.1 mmHg (lit.)
density
1.027 g/mL at 20 °C (lit.)
SMILES string
CC(=O)CCOCc1ccccc1
InChI
1S/C11H14O2/c1-10(12)7-8-13-9-11-5-3-2-4-6-11/h2-6H,7-9H2,1H3
InChI key
BTOZGSIVAZGXCH-UHFFFAOYSA-N
General description
4-Benzyloxy-2-butanone on aminophosphonylation followed by cyclization yields 3-amino-2-oxo-1,2-oxaphospholane.
Application
4-Benzyloxy-2-butanone was used in the synthesis of 4-benzyloxy-2-butanol.
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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.
Synthesis of 3-amino-2-oxo-1, 2-oxaphospholanes and 3-amino-2-oxo-1, 2-oxaphosphorinanes.
Finet J, et al.
Phosph. Sulfur Relat. Elem., 81(1-4), 17-25 (1993)
Reductive cleavage of acetals and ketals by Borane.
Fleming B and Bolker HI.
Canadian Journal of Chemistry, 52(6), 888-893 (1974)
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