161168-55-4 Usage
Amino acid derivative
It is a modified version of an amino acid, which are the building blocks of proteins.
Two amino groups
These functional groups (-NH2) contribute to the compound's reactivity and its ability to form bonds with other molecules.
Methyl group
The presence of a CH3 group in the compound affects its chemical properties and reactivity.
Building block in synthesis
It is commonly used as a starting material for creating pharmaceuticals and other organic compounds due to its versatile chemical structure.
Potential applications in neurological disorders
Research has been conducted on its possible therapeutic effects for conditions affecting the nervous system.
Anticonvulsant properties
The compound has been studied for its potential to help prevent or treat seizures and other convulsive disorders.
Treatment of muscle disorders
2-AMINO-2-METHYL-3-METHYLAMINO-PROPANOIC ACID has been investigated for its possible benefits in addressing muscle-related conditions.
Dietary supplement ingredient
Its potential inclusion in dietary supplements suggests that it may have health benefits or performance-enhancing effects when ingested.
Check Digit Verification of cas no
The CAS Registry Mumber 161168-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,6 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 161168-55:
(8*1)+(7*6)+(6*1)+(5*1)+(4*6)+(3*8)+(2*5)+(1*5)=124
124 % 10 = 4
So 161168-55-4 is a valid CAS Registry Number.
161168-55-4Relevant articles and documents
Preparation of (R)- and (S)-2-Alkyl-2-amino-3-(methylamino)propanoic and Other 2,3-Diaminoalkanoic Acid Derivatives from a Chiral Imidazoline
Pfammatter, Elmar,Seebach, Dieter
, p. 1323 - 1336 (2007/10/02)
t-Butyl 2-t-butyl-3-methyl-4-oxo-1-imidazolidinecarboxylate (Boc-BMI, 1) is deoxygenated (->3), reductively carboxylated (->10, 11), converted to an imidazolinedicarboxylate 31 and subjected to a 1,2-carbonyl-group transposition (->34).The new chiral building blocks thus obtained are used to synthesize derivatives of (i) 1,2-ethylenediamines (type 4-11), of diaminopropanols (8, 16-18) via the lithiated carbamate F, (ii) of 2-alkyl-2,3-diaminopropanoic acid (20-26, 30) via the enolate H, (iii) of higher 2,3-diaminoalkanoic acids (see 32, 33) via the Michael acceptor 31, and (iv) of simple α-(methylamino) acids (type 35) via the enolate of 34.A number of free α,β-diaminocarboxylic acids with a tertiary stereogenic center in the α-position is prepared (37 - 39).Some of these diamino acids are cyclized to β-lactams (41 - 43) bearing an alkyl and a phenylsulfonylamido group in the 2-position.Key Words: Imidazolidine, chiral, building block for amino acids / Ethylenediamines, enantioselective synthesis of / Carbamates, lithiated / Cuprate Michael additions / α,β-Diaminopropanoic acids, α-branched / β-Lactams / Amino acids
