13750-57-7 Usage
Description
(E)-1-Pyrrolidino-2-pentene, also known as N-allylpyrrolidine or NAP, is an organic compound that serves as a versatile intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is a clear, colorless liquid with a strong, pungent odor, and it is highly flammable. Being insoluble in water but soluble in organic solvents, NAP is recognized for its reactivity and utility in the production of a wide range of chemical compounds.
Uses
Used in Pharmaceutical Industry:
(E)-1-Pyrrolidino-2-pentene is used as a key intermediate for the synthesis of pharmaceuticals, including the anti-epileptic drug levetiracetam. Its role in the creation of essential medications highlights its importance in this industry.
Used in Agrochemical Industry:
NAP is also utilized as a building block in the synthesis of herbicides and pesticides. Its contribution to the development of these products underscores its significance in the agricultural sector, where it helps to increase crop yields and protect plants from harmful organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 13750-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13750-57:
(7*1)+(6*3)+(5*7)+(4*5)+(3*0)+(2*5)+(1*7)=97
97 % 10 = 7
So 13750-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H17N/c1-3-9(4-2)10-7-5-6-8-10/h3H,4-8H2,1-2H3/b9-3+
13750-57-7Relevant articles and documents
Novel process for the production of 4,6-dimethyl-7-hydroxynonan-3-one
-
, (2008/06/13)
A process for the production of 4,6-dimethyl-7-hydroxynonan-3-one of specific stereochemistry is disclosed. The process results in an active (+)-serricornin.
Optimum Conditions for Enamine Synthesis by an Improved Titanium Tetrachloride Procedure
Carlson, Rolf,Nilsson, Asa,Stroemqvist, Mats
, p. 7 - 14 (2007/10/02)
A modified procedure for enamine synthesis which results in shorter times and increased yield has been developed.Optimum conditions for the synthesis have been obtained from a series of eight different acyclic ketones with three different amines.The optimum conditions were determined either by response surface methodologgy or by simplex technique.In view of the results some consideration of the mechanism is briefly discussed.
