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Acetic acid, 2-nitro-, 1,1-dimethylethyl ester, also known as 2-nitroacetate, is a colorless to pale yellow liquid with a fruity odor and is highly flammable. It is classified as an acetic acid ester and is commonly used in the production of organic chemicals and as a solvent in various industrial processes. It is important to handle this chemical with care, as exposure to high concentrations can cause irritation to the eyes, skin, and respiratory system. Additionally, it is a potential environmental hazard and should be handled and disposed of properly to prevent harm to the ecosystem.

18598-93-1

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18598-93-1 Usage

Uses

Used in Pesticide Industry:
Acetic acid, 2-nitro-, 1,1-dimethylethyl ester is used as a pesticide and insect repellent for controlling pests and insects in agricultural and residential settings.
Used in Organic Chemical Production:
Acetic acid, 2-nitro-, 1,1-dimethylethyl ester is used in the production of organic chemicals due to its versatile chemical properties.
Used as a Solvent in Industrial Processes:
Acetic acid, 2-nitro-, 1,1-dimethylethyl ester is used as a solvent in various industrial processes, such as in the manufacturing of paints, coatings, and adhesives, due to its ability to dissolve a wide range of substances.

Check Digit Verification of cas no

The CAS Registry Mumber 18598-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,9 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18598-93:
(7*1)+(6*8)+(5*5)+(4*9)+(3*8)+(2*9)+(1*3)=161
161 % 10 = 1
So 18598-93-1 is a valid CAS Registry Number.

18598-93-1Downstream Products

18598-93-1Relevant academic research and scientific papers

THE REACTION OF CARBANIONS WITH 2-SUBSTITUTED -2-NITROPROPANES SUBSTITUTION AND DIMERIZATION OCCURRING BY RADICAL CHAIN PROCESSES INVOLVING ELECTRON TRANSFER

Russell, Glen A.,Mudryk, Boguslaw,Ros, Francisco,Jawdosiuk, Mikolaj

, p. 1059 - 1068 (1982)

The reaction of mono-enolate anions with O2NCMe2X where X=Cl, NO2, p-MePhSO2 yield coupling (RCOCH(R')(CMe2NO2) and enolate dimerization products (RCOCH(R')CH(R')COR) by free radical chain mechanisms involving bimolecular substitution or electron transfer reactions between the enolate anion and the intermediate nitro alkane radical anion (XCMe2NO2(1-)).

Domino processes as a tool for recovering substandard reactions. Synthesis and use of nitroacetic acid esters and amides

Scardovi, Noemi,Casalini, Andrea,Peri, Francesca,Righi, Paolo

, p. 965 - 968 (2007/10/03)

(equation presented) Elusive nitroacetic acid esters and amides were obtained through a halogen exchange reaction of the corresponding bromoacetic acid derivatives with polymer-supported nitrite anion. The process is flawed by a side product catalyzed deg

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