2696-85-7 Usage
Description
2-N-BUTYLANILINE, with the molecular formula C10H15N, is a pale yellow liquid chemical compound characterized by a faint amine odor. It serves as a versatile intermediate in the synthesis of dyes, pigments, and organic compounds, and also finds applications in corrosion inhibition, polymer stabilization, and as a potential antioxidant in various industrial formulations.
Uses
Used in Chemical Synthesis Industry:
2-N-BUTYLANILINE is used as an intermediate for the production of various dyes and pigments, contributing to the coloration and enhancement of numerous products.
Used in Organic Compound Synthesis:
It is utilized in the synthesis of organic compounds, playing a crucial role in the creation of a wide range of chemical products.
Used in Metalworking Fluids:
2-N-BUTYLANILINE is used as a corrosion inhibitor in metalworking fluids, helping to protect metal surfaces from degradation and wear during manufacturing processes.
Used in Polymer and Fuel Industries:
It serves as a stabilizer for polymers and fuels, enhancing the longevity and performance of these materials in various applications.
Used in Antioxidant Formulations:
Due to its potential antioxidant properties, 2-N-BUTYLANILINE is used in the formulation of antioxidant additives for industrial applications, providing protection against oxidative degradation and extending the service life of products.
It is important to handle 2-N-BUTYLANILINE with care, as it can be harmful if ingested, inhaled, or if it comes into contact with the skin, highlighting the need for proper safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 2696-85-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,9 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2696-85:
(6*2)+(5*6)+(4*9)+(3*6)+(2*8)+(1*5)=117
117 % 10 = 7
So 2696-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N/c1-2-3-6-9-7-4-5-8-10(9)11/h4-5,7-8H,2-3,6,11H2,1H3
2696-85-7Relevant articles and documents
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Gassman,Gruetzmacher
, p. 588 (1973)
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Structural development of liver X receptor (LXR) antagonists derived from thalidomide-related glucosidase inhibitors
Noguchi-Yachide, Tomomi,Miyachi, Hiroyuki,Aoyama, Hiroshi,Aoyama, Atsushi,Makishima, Makoto,Hashimoto, Yuichi
, p. 1750 - 1754 (2008/09/17)
Following our previous discovery of LXR antagonistic activity of 2′-substituted phenylphthalimides derived from thalidomide-related glucosidase inhibitors, structure-activity studies and further structural development led to 5-chloro-N-2′-n-pentylphenyl-1,3-dithiophthalimide (5CPPSS-50), with IC50 values of about 10 and 13 μM for LXRα and LXR β, respectively.
Para-bromination of ortho-alkyl anilines
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, (2008/06/13)
A process of selectively preparing p-bromo-o-alkylanilines (e.g. 4-bromo-2-methylaniline) by reacting o-alkylanilines (e.g., 2-methylaniline) with unadsorbed bromine in a solvent selected from the group consisting of an inert di- tri- or tetrahaloaliphatic hydrocarbon (e.g., dichloromethane and dibromomethane), an alkyl nitrile (e.g., acetonitrile) and mixtures thereof.
