264254-04-8 Usage
Description
[1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE, also known as 1,4-Dioxane-2-ylmethylmethylamine, is a heterocyclic organic compound with the molecular formula C5H11NO2. It is a derivative of dioxane and is known for its nucleophilic properties in various chemical reactions. [1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE has potential applications in the pharmaceutical and agrochemical industries, but it is also classified as a hazardous substance with potential environmental and health risks, including carcinogenic effects.
Uses
Used in Organic Synthesis:
[1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE is used as a nucleophilic agent in various organic synthesis reactions due to its ability to donate electron pairs and form new chemical bonds.
Used in Pharmaceutical Industry:
[1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE is used as a chemical intermediate in the development of pharmaceutical compounds, contributing to the synthesis of potential drug candidates.
Used in Agrochemical Industry:
[1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides, due to its reactivity and potential to form biologically active molecules.
However, it is important to note that the use and handling of [1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE should be carefully managed to minimize potential risks associated with its classification as a hazardous substance and its potential carcinogenic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 264254-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,2,5 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 264254-04:
(8*2)+(7*6)+(6*4)+(5*2)+(4*5)+(3*4)+(2*0)+(1*4)=128
128 % 10 = 8
So 264254-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO2/c1-7-4-6-5-8-2-3-9-6/h6-7H,2-5H2,1H3
264254-04-8Relevant articles and documents
Synthesis of mono- and bis(aminomethyl)dioxanes from N-[3-(2-chloroethoxy)-2-hydroxypropyl]sulfamates
Bulatov,Ermakov,Tartakovsky
, p. 2299 - 2301 (1999)
N-Substituted aminomethyl- and 2,5-bis(aminomethyl)-1,4-dioxanes were prepared by cyclization of the corresponding potassium N-[3-(2-chloroethoxy)-2-hydroxypropyl]sulfamates under the action of an alkaline agent followed by alcoholysis of the resulting su
TYROSINE KINASE INHIBITORS
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, (2008/06/13)
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