54035-94-8 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-Bromoethyl)-pyrrolidine is used as a building block for the synthesis of various pharmaceuticals due to its ability to participate in multiple chemical reactions, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 1-(2-Bromoethyl)-pyrrolidine serves as a key component in the creation of different agrochemicals, aiding in the advancement of products for agricultural applications.
Used in Organic Synthesis:
1-(2-Bromoethyl)-pyrrolidine is utilized as a versatile reagent in organic synthesis, enabling the production of a wide array of organic compounds for diverse applications across various industries.
Used in Chemical Research:
As a component of chemical research, 1-(2-Bromoethyl)-pyrrolidine is employed to explore and understand various chemical reactions and transformations, furthering scientific knowledge and potentially leading to innovative applications.
Check Digit Verification of cas no
The CAS Registry Mumber 54035-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,3 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54035-94:
(7*5)+(6*4)+(5*0)+(4*3)+(3*5)+(2*9)+(1*4)=108
108 % 10 = 8
So 54035-94-8 is a valid CAS Registry Number.
54035-94-8Relevant academic research and scientific papers
Endothelin antagonists
-
, (2008/06/13)
A compound of the formula (I): or a pharmaceutically acceptable salt thereof is disclosed, as well as processes for and intermediates in the preparation thereof, and a method of antagonizing endothelin.
Chiral synthesis for producing 1-azabicyclo[2.2.1] heptane-3-carboxylates
-
, (2008/06/13)
A process for preparing substantially pure enantiomers of formula (I) STR1 where the * represents a chiral center, x is 0 or 1, in exo-, endo- or a mixture of exo- and endo- forms; and R is hydrogen, alkyl or aralkyl, via diastereomers of formula (IIA) or
