208922
Ethyl acetohydroxamate
97%
동의어(들):
Ethyl N-hydroxyacetimidate, Ethyl acetohydroximate
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3C(=NOH)OC2H5
CAS 번호:
Molecular Weight:
103.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
234-165-7
Beilstein/REAXYS Number:
1700260
MDL number:
Assay:
97%
InChI key
QWKAVVNRCKPKNM-SNAWJCMRSA-N
InChI
1S/C4H9NO2/c1-3-7-4(2)5-6/h6H,3H2,1-2H3/b5-4+
SMILES string
CCO\C(C)=N\O
assay
97%
greener alternative product score
old score: 6
new score: 5
Find out more about DOZN™ Scoring
greener alternative product characteristics
Waste Prevention
Safer Solvents and Auxiliaries
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
refractive index
n20/D 1.434 (lit.)
bp
55-58 °C/6 mmHg (lit.)
mp
23-25 °C (lit.)
functional group
amine, ether, oxime
greener alternative category
storage temp.
2-8°C
Quality Level
General description
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Waste Prevention”, “Safer Solvents and Auxiliaries” and “Enhanced Energy Efficiency”. Click here to view its DOZN scorecard.
Application
Ethyl acetohydroxamate was used in the synthesis of:
- O-acyl-and O-nitrophenylhydroxylamines
- hydroxamic acid ethoxycarbonylhydrazides
- ethyl O-(2,4-dinitrophenyl)acetohydroxamate
Tetrahedron, 40, 3769-3769 (1984)
Sigmatropic Rearrangements of 2, 4-Dinitrophenyl Oximes.
Boyle PH, et al.
ARKIVOC (Gainesville, FL, United States), 7, 67-79 (2003)
Synthesis and some properties of O-acyl-and O-nitrophenylhydroxylamines.
Y Tamura et al.
The Journal of organic chemistry, 38(6), 1239-1241 (1973-03-23)
Synthesis of 4-hydroxy-4, 5-dihydro-1, 2, 4-triazol-5-ones.
Ikizler AA and Sancak K.
Monatshefte fur Chemie / Chemical Monthly, 123(3), 257-263 (1992)
J Stanek et al.
Journal of medicinal chemistry, 35(8), 1339-1344 (1992-04-17)
1-Amino-3-(aminooxy)-2-propanol (6a) has been synthesized and found to inhibit rat liver ornithine decarboxylase (ODC) with an IC50 in the nanomolar range. Compound 6a served as a basis for the design of new enzyme inhibitors, which led to the identification of
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