4879-95-2 Usage
Description
Beta-Isovalerolactam, also known as bivalactam, is a heterocyclic compound with the molecular formula C5H9NO. It is a cyclic amide, specifically a lactam, and is known for its unique chemical properties. This versatile compound is widely recognized for its role as a precursor in the synthesis of pharmaceuticals and agrochemicals, as well as an intermediate in the production of polymers like nylon. Furthermore, it has garnered interest for its potential as a chiral catalyst in organic chemistry reactions.
Uses
Used in Pharmaceutical and Agrochemical Industries:
Beta-Isovalerolactam is utilized as a precursor in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its unique chemical structure allows it to be a key component in creating molecules with specific therapeutic or pesticidal properties.
Used in Polymer Production:
As an intermediate in the production of polymers, Beta-Isovalerolactam plays a crucial role in the manufacturing process of materials like nylon. Its involvement in polymer chemistry aids in the creation of versatile and durable polymers used in a wide range of applications, from textiles to engineering plastics.
Used in Organic Chemistry Research:
Beta-Isovalerolactam has been studied for its potential as a chiral catalyst in organic chemistry reactions. Its unique properties make it a promising candidate for enhancing the selectivity and efficiency of various chemical processes, leading to advancements in the synthesis of enantiomerically pure compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 4879-95-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4879-95:
(6*4)+(5*8)+(4*7)+(3*9)+(2*9)+(1*5)=142
142 % 10 = 2
So 4879-95-2 is a valid CAS Registry Number.
4879-95-2Relevant articles and documents
NEW METHODS FOR β-LACTAM FORMATION FROM β-AMINO ACIDS USING (C6H5)3/CCl4 AND (C6H5)3P/NBS
Kim, Sunggak,Lee, Phil Ho,Lee, Tai Au
, p. 247 - 252 (2007/10/02)
Triphenylphosphine/carbon tetrachloride and triphenylphosphine/N-bromosuccinimide were found to be very effective for β-lactam formation from β-amino acids in acetonitrile.
Selective Hydrogenation of 4,5-Dihydro-1,3-oxazin-6-ones to Carbaldehyde Derivatives; Chemical Differentiation between Acylazetidin-2-ones and the Corresponding Isomeric Oxazin-6-ones
Drey, Charles N. C.,Ridge, Richard J.,Mtetwa, Eli
, p. 378 - 380 (2007/10/02)
Catalytic hydrogenation of optically active and non-active dihydro-oxazin-6-ones unexpectedly led to preferential reduction of the carbonyl group with ring-opening yielding carbaldehyde derivatives.This reaction resolved a structural problem by leading to
