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3-(MethoxyMethoxy)propanenitrile, also known as 3-Methoxy-3-methoxypropanenitrile, is a colorless liquid chemical compound with the molecular formula C6H11NO2 and a strong, pungent odor. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
3-(MethoxyMethoxy)propanenitrile is used as a building block for the synthesis of various organic compounds, such as esters and amides, which are essential in the development of new pharmaceuticals.
Used in Agrochemical Industry:
3-(MethoxyMethoxy)propanenitrile is used as a chemical intermediate in the production of agrochemicals, contributing to the development of effective and safe products for agricultural applications.
Used in Chemical Reactions:
3-(MethoxyMethoxy)propanenitrile is used as a solvent in chemical reactions, facilitating the synthesis of various organic compounds and aiding in the production process.
Used in Production of Other Compounds:
3-(MethoxyMethoxy)propanenitrile is used as a chemical intermediate in the production of other compounds, expanding its applications in various industries and research fields.
It is important to handle 3-(MethoxyMethoxy)propanenitrile with care, as it can be toxic if ingested or inhaled, and can also irritate the skin and eyes upon contact.

52406-33-4

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52406-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52406-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,0 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52406-33:
(7*5)+(6*2)+(5*4)+(4*0)+(3*6)+(2*3)+(1*3)=94
94 % 10 = 4
So 52406-33-4 is a valid CAS Registry Number.

52406-33-4Relevant academic research and scientific papers

Synthesis of the Sex Pheromone of the Oleander Scale (Aspidiotus nerii)

Casta?eda, Mary Monta?o,Bargues, Javier Marzo,Primo, Jaime,Fuertes, Ismael Navarro

, p. 8578 - 8588 (2019)

A total synthesis of the oleander scale [Aspidiotus nerii (Bouche)] sex pheromone, the unique sesquiterpenoid containing a cyclobutane moiety of this class of compounds, has been developed. In order to implement this sex pheromone as a new environmentally

Using nucleophilic substitution reactions to understand how a remote alkyl or alkoxy substituent influences the conformation of eight-membered ring oxocarbenium ions

Chamberland, Stephen,Woerpel

, p. 4739 - 4741 (2007/10/03)

(Chemical Equation Presented) A remote alkoxy substituent strongly stabilizes one particular conformer of an eight-membered ring oxocarbenium ion by a through-space electrostatic effect. X-ray crystallographic analysis of a crystalline derivative proves t

Stereoselectivity of Electrophile-Promoted Cyclizations of γ-Hydroxyalkenes. An Investigation of Carbohydrate-Derived and Model Substrates

Reitz, Allen B.,Nortey, Samuel O.,Maryanoff, Bruce E.,Liotta, Dennis,Robert, Monahan

, p. 4191 - 4202 (2007/10/02)

We have investigated cyclization reactions of γ-hydroxyalkenes bearing an alkoxy or alkyl substituent on the allylic carbon.A variety of electrophiles N-bromosuccinimide, N-iodosuccinimide, iodine, mercury(II) acetate, mercury(II) trifluoroacetate, mercu

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