40221-52-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
CYCLOOCTYLMETHYLAMINE serves as a building block in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides.
Used as a Corrosion Inhibitor:
In industrial settings, CYCLOOCTYLMETHYLAMINE is employed as a corrosion inhibitor to protect metal surfaces from degradation, extending the lifespan of equipment and structures.
Used as a Flotation Agent in Mining:
In the mining industry, CYCLOOCTYLMETHYLAMINE functions as a flotation agent, aiding in the separation of valuable minerals from waste materials through the flotation process.
Used as a Chemical Intermediate in Surfactant and Lubricant Production:
CYCLOOCTYLMETHYLAMINE is utilized as a chemical intermediate in the manufacturing of surfactants and lubricants, enhancing the performance and efficiency of these products.
Used in the Manufacture of Dyes, Pigments, and Polymer Additives:
CYCLOOCTYLMETHYLAMINE also finds application in the production of dyes, pigments, and polymer additives, contributing to the coloration and functional properties of various materials.
However, due to its toxicity and potential hazards to human health and the environment, CYCLOOCTYLMETHYLAMINE should be handled with care and proper safety measures should be implemented during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 40221-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40221-52:
(7*4)+(6*0)+(5*2)+(4*2)+(3*1)+(2*5)+(1*2)=61
61 % 10 = 1
So 40221-52-1 is a valid CAS Registry Number.
40221-52-1Relevant academic research and scientific papers
Photometric Characterization of the Reductive Amination Scope of the Imine Reductases from Streptomyces tsukubaensis and Streptomyces ipomoeae
Matzel, Philipp,Krautschick, Lukas,H?hne, Matthias
, p. 2022 - 2027 (2017/10/07)
Imine reductases (IREDs) have emerged as promising enzymes for the asymmetric synthesis of secondary and tertiary amines starting from carbonyl substrates. Screening the substrate specificity of the reductive amination reaction is usually performed by time-consuming GC analytics. We found two highly active IREDs in our enzyme collection, IR-20 from Streptomyces tsukubaensis and IR-Sip from Streptomyces ipomoeae, that allowed a comprehensive substrate screening with a photometric NADPH assay. We screened 39 carbonyl substrates combined with 17 amines as nucleophiles. Activity data from 663 combinations provided a clear picture about substrate specificity and capabilities in the reductive amination of these enzymes. Besides aliphatic aldehydes, the IREDs accepted various cyclic (C4–C8) and acyclic ketones, preferentially with methylamine. IR-Sip also accepted a range of primary and secondary amines as nucleophiles. In biocatalytic reactions, IR-Sip converted (R)-3-methylcyclohexanone with dimethylamine or pyrrolidine with high diastereoselectivity (>94–96 % de). The nucleophile acceptor spectrum depended on the carbonyl substrate employed. The conversion of well-accepted substrates could also be detected if crude lysates were employed as the enzyme source.
