2696-85-7 Usage
General Description
2-N-BUTYLANILINE is a chemical compound with the molecular formula C10H15N. It is a pale yellow liquid with a faint amine odor. It is primarily used as an intermediate in the production of various dyes and pigments, as well as in the synthesis of organic compounds. It is also utilized as a corrosion inhibitor in metalworking fluids, and as a stabilizer for polymers and fuels. In addition, 2-N-BUTYLANILINE has been found to possess potential antioxidant properties, making it useful in the formulation of antioxidant additives for various industrial applications. However, it is important to handle this chemical with care as it can be harmful if ingested, inhaled, or if it comes into contact with the skin.
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.
