H55405
4′-Hydroxypropiophenone
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
HOC6H4COC2H5
CAS Number:
Molecular Weight:
150.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-743-2
Beilstein/REAXYS Number:
907511
MDL number:
Assay:
98%
Quality Level
assay
98%
mp
147.5-148.5 °C (lit.)
SMILES string
CCC(=O)c1ccc(O)cc1
InChI
1S/C9H10O2/c1-2-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3
InChI key
RARSHUDCJQSEFJ-UHFFFAOYSA-N
Still not finding the right product?
Explore all of our products under 4′-Hydroxypropiophenone
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
H55405-500G: + H55405-VAR: + H55405-BULK: + H55405-5KG: + H55405-100G:
jan
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.
p-Hydroxypropiophenone effects on azo dye-induced alterations in mouse hepatic cells: light and electron microscopic study.
N J Unakar
Journal of the National Cancer Institute, 44(4), 873-891 (1970-04-01)
A Tanner et al.
Journal of bacteriology, 182(23), 6565-6569 (2000-11-14)
An arylketone monooxygenase was purified from Pseudomonas putida JD1 by ion exchange and affinity chromatography. It had the characteristics of a Baeyer-Villiger-type monooxygenase and converted its substrate, 4-hydroxyacetophenone, into 4-hydroxyphenyl acetate with the consumption of one molecule of oxygen and
Zack E Bryant et al.
Bioorganic & medicinal chemistry letters, 21(3), 912-915 (2011-01-14)
A series of ethacrynic acid analogues, lacking the α,β-unsaturated carbonyl unit, was synthesized and subsequently evaluated for their ability to inhibit the migration of human breast cancer cells, Hs578Ts(i)8 as well as of human prostate cancer cells, C4-2B. These cell