4088-36-2 Usage
General Description
Decan-3-amine, also designated by IUPAC as N-Decan-3-amine, is a primary aliphatic amine that has a carbon length of ten and is classified as a liquid. Its formula is C10H23N, and it is characterized by an irregular, fishy smell. This substance is less dense than water and insoluble in the water but soluble in many organic solvents. It reacts violently with strong oxidizers and can cause burns and severe eye and skin irritation. In industrial applications, Decan-3-amine is used in the manufacturing of detergents, emulsifiers, and corrosion inhibitors.
Check Digit Verification of cas no
The CAS Registry Mumber 4088-36-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4088-36:
(6*4)+(5*0)+(4*8)+(3*8)+(2*3)+(1*6)=92
92 % 10 = 2
So 4088-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H23N/c1-3-5-6-7-8-9-10(11)4-2/h10H,3-9,11H2,1-2H3
4088-36-2Relevant articles and documents
Synthesis of Dialkylamines via the Reaction of Organoboranes with N-Chloroalkylamines
Kabalka, George W.,McCollum Gary W.,Kunda, Sastry A.
, p. 1656 - 1658 (1984)
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Hydrosilylative reduction of primary amides to primary amines catalyzed by a terminal [Ni-OH] complex
Pandey, Pragati,Bera, Jitendra K.
supporting information, p. 9204 - 9207 (2021/09/20)
A terminal [Ni-OH] complex1, supported by triflamide-functionalized NHC ligands, catalyzes the hydrosilylative reduction of a range of primary amides into primary amines in good to excellent yields under base-free conditions with key functional group tolerance. Catalyst1is also effective for the reduction of a variety of tertiary and secondary amides. In contrast to literature reports, the reactivity of1towards amide reduction follows an inverse trend,i.e., 1° amide > 3° amide > 2° amide. The reaction does not follow a usual dehydration pathway.
