19977-51-6 Usage
Description
Piperidine, 1-(3-bromo-2-propynyl)is a piperidine derivative featuring a bromoalkyne group attached to its nitrogen atom. This chemical compound is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and organic materials, serving as a versatile building block for creating various drugs and bioactive compounds.
Uses
Used in Pharmaceutical Industry:
Piperidine, 1-(3-bromo-2-propynyl)is used as a building block for the synthesis of various drugs and bioactive compounds, contributing to the development of new medications and therapies.
Used in Organic Synthesis:
Piperidine, 1-(3-bromo-2-propynyl)is used as a reagent in organic synthesis, facilitating the creation of a range of chemical products through its reactive bromoalkyne group.
Used in Agrochemical Industry:
Due to its chemical structure and reactivity, Piperidine, 1-(3-bromo-2-propynyl)has potential use as a pesticide or herbicide, offering a foundation for developing effective agricultural chemicals.
Used in Preparation of Chemical Products:
Piperidine, 1-(3-bromo-2-propynyl)serves as a starting material for the preparation of various chemical products, expanding its applications beyond the pharmaceutical and agrochemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 19977-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,7 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19977-51:
(7*1)+(6*9)+(5*9)+(4*7)+(3*7)+(2*5)+(1*1)=166
166 % 10 = 6
So 19977-51-6 is a valid CAS Registry Number.
19977-51-6Relevant articles and documents
HYDROBORATION D'AMINES INSATUREES. V. NOUVELLE VOIE D'ACCES AUX AMIOALKYLIDENECYCLOALKANES
Torregrosa, Jean-Luc,Baboulene, Michel,Speziale, Vincent,Lattes, Armand
, p. 311 - 318 (2007/10/02)
Hydroboration of various 1-bromopropargylamines by borinane and 3,6-dimethylborepane has led to α-bromovinylboranes.Treatment of these compounds with iodine in basic media, only gives aminoalkylidenecycloalkanes with excellent yields.