21404-88-6 Usage
General Description
2-Methyl-2-phenylpropan-1-amine is a chemical compound that is made up of carbon, hydrogen, and nitrogen atoms. Known as an organic compound, its structure contains both a phenyl and an amine group. Alongside, it also has a tertiary carbon atom, which is an atom of carbon attached to three other carbon atoms. It doesn't have extensive commercial or industrial uses and can be synthesized in a laboratory. Its properties would be greatly influenced by its structural characteristics, such as being a derivative of propane and having both a phenyl ring and an amine group in its structure. Additional studies and handling must adhere to standard safety protocols for chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 21404-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,0 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21404-88:
(7*2)+(6*1)+(5*4)+(4*0)+(3*4)+(2*8)+(1*8)=76
76 % 10 = 6
So 21404-88-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N/c1-10(2,8-11)9-6-4-3-5-7-9/h3-7H,8,11H2,1-2H3
21404-88-6Relevant articles and documents
Nitrile Synthesis by Aerobic Oxidation of Primary Amines and in situ Generated Imines from Aldehydes and Ammonium Salt with Grubbs Catalyst
Utsumi, Tatsuki,Noda, Kenta,Kawauchi, Daichi,Ueda, Hirofumi,Tokuyama, Hidetoshi
, p. 3583 - 3588 (2020/08/05)
Herein, a Grubbs-catalyzed route for the synthesis of nitriles via the aerobic oxidation of primary amines is reported. This reaction accommodates a variety of substrates, including simple primary amines, sterically hindered β,β-disubstituted amines, allylamine, benzylamines, and α-amino esters. Reaction compatibility with various functionalities is also noted, particularly with alkenes, alkynes, halogens, esters, silyl ethers, and free hydroxyl groups. The nitriles were also synthesized via the oxidation of imines generated from aldehydes and NH4OAc in situ. (Figure presented.).
Sympathetic nervous system blocking agents. V. Derivatives of isobutyl-, t-butyl-, and neopentylguanidine.
Short,Ours,Ranus Jr.
, p. 1129 - 1135 (2007/10/05)
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