54162-90-2 Usage
Chemical Properties
BEIGE FINE POWDER
Purification Methods
Purify the free amino-acid by dissolving it in H2O and passing it through a Dowex 50W (acid form) column and eluting with 1M aqueous NH4OH. The eluate is evaporated (in vacuo) and the residue is dissolved in H2O. Me2CO is added to turbidity, cooled at 0o and the colourless crystals of the amino-acid are collected and dried in vacuo [Bernáth et al. Tetrahedron 41 1315 1958, cf Mazza & Crapetta Gazzetta 57 297 1927]. In earlier work, it was recrystallised from aqueous EtOH and had reported melting points of 265-265o [Kricheldorf Justus Liebigs Ann Chem 1378 1975] and 269-271o [Marconi & Mazzochi J Org Chem 31 1372 1966]. The hydrochloride [57266-56-5] M 177.6 has m 210-213o and the methyl ester hydrochloride [52766-61-2] has m 85-87o (from Et2O). The trans-(±)-(1RS,2RS)-amino-acid [97945-19-2] crystallises from aqueous Me2CO with m 267-269o. [Beilstein 14 II 203.]
Check Digit Verification of cas no
The CAS Registry Mumber 54162-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,6 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54162-90:
(7*5)+(6*4)+(5*1)+(4*6)+(3*2)+(2*9)+(1*0)=112
112 % 10 = 2
So 54162-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-2,5-6H,3-4,8H2,(H,9,10)/t5-,6+/m1/s1
54162-90-2Relevant articles and documents
A convenient Hofmann reaction of carboxamides and cyclic imides mediated by trihaloisocyanuric acids
Bastos, Gustavo A.,de Mattos, Marcio C.S.
, (2021/09/29)
A simple, efficient and pot-economic approach in a single vessel has been developed for conversion of aromatic and aliphatic carboxamides into primary amines with one fewer carbom atom (Hofmann reaction) in 38–89 % yield by reacting with trichloro- or tribromoisocyanuric acid and sodium hydroxide in aqueous acetonitrile. Under the same reaction conditions, cyclic imides gave amino acids (69–83 %). The role of the trihaloisocyanuric acids is the in situ generation of N-haloamides, key-intermediates for the Hofmann reaction. The scalability of the methodology was demonstrated by a multigram-scale transformation of phthalimide into anthranilic acid in 77 % yield.
