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[1-Allyl-1-(fluoromethyl)but-3-en-1-yl]amine, an organic compound with the molecular formula C8H14FN, is a primary amine characterized by a terminal double bond and a fluoromethyl group attached to the carbon chain. [1-Allyl-1-(fluoromethyl)but-3-en-1-yl]amine features an allyl group, which consists of three carbon atoms connected by two double bonds, and a but-3-en-1-yl group comprising four carbon atoms with a fluoromethyl substitution. This unique chemical structure and reactivity make it a valuable compound in various applications.

1228552-19-9

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1228552-19-9 Usage

Uses

Used in Organic Synthesis:
[1-Allyl-1-(fluoromethyl)but-3-en-1-yl]amine is used as a building block in organic synthesis for its unique chemical structure and reactivity. It can be employed to create a wide range of complex organic molecules, contributing to the development of new materials and compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, [1-Allyl-1-(fluoromethyl)but-3-en-1-yl]amine is used as a key intermediate in the development of new drugs. Its unique structure allows for the creation of novel drug candidates with potential therapeutic applications.
Used in Agrochemicals:
[1-Allyl-1-(fluoromethyl)but-3-en-1-yl]amine also has potential applications in the agrochemical industry, where it can be used to develop new pesticides, herbicides, or other agricultural chemicals. Its unique chemical properties make it a promising candidate for the creation of innovative products in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 1228552-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,5 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1228552-19:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*5)+(3*2)+(2*1)+(1*9)=149
149 % 10 = 9
So 1228552-19-9 is a valid CAS Registry Number.

1228552-19-9Relevant academic research and scientific papers

New growth regulators of corn based on N-mono- and N,N-bis-3-butenyldichloroacetamides

Bubnov, Yu. N.,Spiridonov, Yu. Ya.,Kuznetsov, N. Yu.

, p. 345 - 358 (2018)

Allylboration of imines, nitriles (including hydrocyanic acid), amides, lactams, aromatic azaheterocycles (pyridines, isoquinoline, and pyrrole) was used to synthesize a series of mono- and bis-3-butenylamines with different structures, which were converted to dichloroacetamides, new analogs of a known safener (herbicide antidote) Dichlormid successfully used in the cultivation of corn throughout the world. Biological tests for the germination of corn seeds showed that most of the dichloroacetamides obtained have growth-stimulating activity, which is mainly directed on the development of the root system. Compounds 2f, trans- and cis-2n, cis-2s, and 2t demonstrated outstanding activity, exceeding from two to three times the stimulating effect of Dichlormid on the developing root system of maize seedlings.

A new method of synthesis of 6-substituted piperidine-2,4-diones from homoallylamines

Kuznetsov, Nikolai Yu.,Maleev, Victor I.,Khrustalev, Victor N.,Mkrtchyan, Anna F.,Godovikov, Ivan A.,Strelkova, Tatyana V.,Bubnov, Yuri N.

experimental part, p. 334 - 344 (2012/02/16)

Mono- and dihomoallylamines serve as convenient precursors for the preparation of 6-substituted piperidine-2,4-diones. This transformation is based, on the one hand, on a simple and well-known halocyclocarbamation reaction proceeding by the addition of a

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