14548-12-0 Usage
Uses
Used in Pharmaceutical Industry:
(1E)-N,N-Dimethyl-1-buten-1-amine is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
DMBA is utilized as an intermediate in the production of agrochemicals, playing a role in the development of pesticides and other agricultural products to enhance crop protection and yield.
Used in Corrosion Inhibition:
(1E)-N,N-Dimethyl-1-buten-1-amine functions as a corrosion inhibitor, helping to protect metal surfaces from degradation and prolonging the lifespan of industrial equipment and structures.
Used in Dye and Pigment Production:
DMBA is employed as a chemical intermediate in the manufacturing of dyes and pigments, contributing to the creation of a wide range of colorants for various applications, including textiles, plastics, and printing inks.
However, it is important to note that DMBA is a hazardous substance with potential health risks. Therefore, it should be handled and stored with caution in a well-ventilated area and using appropriate personal protective equipment to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 14548-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14548-12:
(7*1)+(6*4)+(5*5)+(4*4)+(3*8)+(2*1)+(1*2)=100
100 % 10 = 0
So 14548-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H13N/c1-4-5-6-7(2)3/h5-6H,4H2,1-3H3/b6-5+
14548-12-0Relevant academic research and scientific papers
Triazolines. Part 32. Synthesis of 1-Alkyl-2-aminobenzimidazoles from 5-Amino-1-(2-nitroaryl)-1,2,3-triazolines
Erba, Emanuela,Mai, Giorgio,Pocar, Donato
, p. 2709 - 2712 (2007/10/02)
5-Amino-1-(2-nitroaryl)-1,2,3-triazolines 5 are converted into 1-alkyl-2-aminobenzimidazoles 7 in refluxing triethyl phosphite.The reaction occurs via thermal rearrangement of 5 followed by nitrogen elimination which produces N2-(2-nitroaryl)am