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Ethyl 2-hydroxy-3-nitropropanoate is an organic compound with the chemical formula C5H9NO5. It is a derivative of propanoic acid, featuring a hydroxyl (-OH) group at the 2nd carbon and a nitro (-NO2) group at the 3rd carbon. This molecule is an ester, formed by the reaction of propanoic acid with ethanol, resulting in an ester functional group (-COO-) connecting the two. Ethyl 2-hydroxy-3-nitropropanoate is a colorless liquid with a molecular weight of 163.13 g/mol. It is soluble in water and various organic solvents, and it is used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is important to handle ethyl 2-hydroxy-3-nitropropanoate with care, as it may be sensitive to heat, light, and moisture.

1851-84-9

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1851-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1851-84-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1851-84:
(6*1)+(5*8)+(4*5)+(3*1)+(2*8)+(1*4)=89
89 % 10 = 9
So 1851-84-9 is a valid CAS Registry Number.

1851-84-9Upstream product

1851-84-9Relevant academic research and scientific papers

From Alkenes to Isoxazolines via Copper-Mediated Alkene Cleavage and Dipolar Cycloaddition

Gao, Mingchun,Gan, Yuansheng,Xu, Bin

supporting information, p. 7435 - 7439 (2019/10/08)

An unprecedented copper-mediated anion transformation is reported, along with selective C= C double bond cleavage and dipolar cycloaddition reaction from simple alkenes and inexpensive copper nitrate. Various transformations demonstrate the generality of this method. Further mechanistic investigation indicates a novel ionic pathway for alkene cleavage and highlights the coeffect of iodide and boric acid as additives on the inhibition of well-documented competitive nitration byproducts.

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