34375-90-1 Usage
Uses
Used in Organic Synthesis:
3-Buten-2-amine is used as an intermediate in organic synthesis for the production of various chemicals. Its versatile structure allows it to be a key component in the synthesis of pharmaceuticals, pesticides, and surfactants, making it valuable in the chemical industry.
Used in Aroma Production:
3-Buten-2-amine is found in the essential oils of some plants and is identified as a volatile compound responsible for the aroma of certain fruits and flowers. It is used in the fragrance industry to create natural and appealing scents for various products.
Used in Chemical Production:
As an important intermediate, 3-Buten-2-amine is used in the production of various chemicals, including pharmaceuticals, pesticides, and surfactants. Its presence in these products is crucial for their effectiveness and performance in their respective applications.
Check Digit Verification of cas no
The CAS Registry Mumber 34375-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,7 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34375-90:
(7*3)+(6*4)+(5*3)+(4*7)+(3*5)+(2*9)+(1*0)=121
121 % 10 = 1
So 34375-90-1 is a valid CAS Registry Number.
34375-90-1Relevant academic research and scientific papers
The Reactions of Singlet NH Radicals with C4 Olefins in the Liquid Phase
Hamada, Jun-ichi,Tsunashima, Shigeru,Sato, Shin
, p. 662 - 666 (2007/10/02)
The reactions of NH radicals with C4 olefins, trans- and cis-2-butenes, 1-butene, and isobutene, were investigated by the photolysis of hydrogen azide in the liquid olefin at 0 deg C and at the temperature of Dry Ice-methanol.Except for nitrogen and ammonia, amines and aziridines were found to be formed in good yield. 2-Butene-1-amine and trans-2,3-dimethylaziridine from trans-2-butene, 2-butene-1-amine and cis-2,3-dimethylaziridine from cis-2-butene, 3-butene-1- and 2-amines and 2-ethylaziridine from 1-butene, and 2-methyl-2-propene-1-amine and 2,2-dimethylaziridine from isobutene.These product formations were successfully explained by the insertion into the C-H bond and the addition to the double bond of olefin by the singlet NH radicals.In the case of 2-butene, no isomerized aziridine formation was observed.This result suggested that the triplet NH radicals rarely add to the double bond of olefin.
