2156-71-0 Usage
Uses
Used in Chemical Production:
NISTC2156710 is used as a chemical intermediate for the synthesis of various chemicals, including butyric acid, butyl acetate, and butyl amines. Its versatility as a building block in chemical reactions makes it valuable in the production of numerous industrial products.
Used in Solvent Applications:
As a solvent, NISTC2156710 is utilized in the manufacturing of coatings, inks, resins, and adhesives. Its ability to dissolve a wide range of substances makes it a preferred choice in these industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, NISTC2156710 is used as a solvent in the production of medications and as a component in the synthesis of various pharmaceutical compounds.
Used in Fuel Additives:
NISTC2156710 is also used as a component in fuel additives, helping to improve the performance and efficiency of fuels.
Used in Flavor and Fragrance Industry:
Due to its strong, sweet odor, NISTC2156710 is employed in the flavor and fragrance industry to create various scents and flavors for consumer products.
Used in Cleaning Products:
NISTC2156710 is used in the formulation of cleaning products, such as detergents and degreasers, due to its ability to dissolve grease and dirt effectively.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, NISTC2156710 is used as a solvent and ingredient in the production of various products, including perfumes, lotions, and creams.
Used in Food and Beverage Industry:
Although it is not intended for direct consumption, NISTC2156710 may be used in the production process of certain food and beverage products, particularly as a component in flavorings and fragrances.
Used in Agricultural Industry:
In agriculture, NISTC2156710 can be used as a solvent in the production of certain agrochemicals, such as herbicides and pesticides, to help control weeds and pests.
Used in Research and Development:
NISTC2156710 is also utilized in research and development settings for the study of chemical reactions and the development of new compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 2156-71-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2156-71:
(6*2)+(5*1)+(4*5)+(3*6)+(2*7)+(1*1)=70
70 % 10 = 0
So 2156-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10ClN/c6-7-4-2-1-3-5-7/h1-5H2
2156-71-0Relevant academic research and scientific papers
Structure-activity considerations in kinetics and mechanism of chlorine exchange between chloramine-T and secondary amines
Dannan,Hussain,Crooks,Dittert
, p. 657 - 660 (2007/10/02)
To study the mechanism of N-chlorination of secondary amines by chloramine-T, the kinetics of the reactions of some aromatic-substituted analogues of N-chlorobenzenesulfonamide with various secondary amines were determined. The importance of amine basicity and reactivity of the N-Cl bond of the N-chlorobenzenesulfonamide was also assessed. The results indicate that a mechanism involving the un-ionized species of both reactants (i.e., a molecular mechanism), rather than an ionic mechanism, is operating and that the reaction most likely proceeds via a six-membered-ring transition state that incorporates a water molecule.
Reaction of Cyclopropanamines with Hypochlorite
Vaidyanathan, Ganesan,Wilson, Joseph W.
, p. 1815 - 1820 (2007/10/02)
Ethylene was formed in 65percent yield when 1-(1-piperidino)cyclopropanol 6, was treated with hypochlorite.This observation raised the possibility that 1-aminocyclopropanecarboxylic acids (ACCs) could yield ethylene by a mechanism that involves (1) decarboxylation to a 1-aminocyclopropanol, followed by (2) a fragmentation of the carbinolamine to ethylene induced by a hypochlorite equivalent.Although this mechanism could be ruled out only for 1e, no evidence could be found for it in the reactions of other ACCs, 1a-f, with hypochlorite.The fact that 1b-cis-2,3-d2 yieldedonly ethylene-cis-1,2-d2 is consistent with either the mechanism described above or a nitrenium ion mechanism.In the reaction of cyclopropanamines with neutral hypochlorite, ethylene is not the major product.From the primary and secondary amino acids 1a-c, a 3-hydroxypropanenitrile or propanamide, 2a-c, probably the product of a nucleophilic ring-opening step followed by decarboxylation, is formed.Similar products are formed from other cyclopropanamines: 2a from 1g, 2d from 1h, 2e and 2f from 1i, and lactone 5 from 1j.
