1482-97-9 Usage
Description
3-Amino-L-alanine hydrochloride, also known as (2S)-2,3-Diaminopropanoic Acid Hydrochloride, is a non-proteinogenic amino acid that exists as a white crystalline powder. It is characterized by its unique chemical structure, which allows it to be used in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
3-Amino-L-alanine hydrochloride is used as a building block for the synthesis of peptides containing non-proteinogenic amino acids. This application is crucial in the development of novel drugs and therapeutic agents, as it enables the creation of unique peptide sequences with potential medicinal properties.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-Amino-L-alanine hydrochloride serves as an important intermediate compound. Its versatile structure allows for the creation of a wide range of chemical products, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
3-Amino-L-alanine hydrochloride is also utilized in research and development settings, where it can be employed to study the properties and functions of non-proteinogenic amino acids. This can lead to a better understanding of their role in biological systems and the potential for developing new therapeutic strategies.
Purification Methods
It forms needles from H2O and can be recrystallised from aqueous EtOH. [Gmelin et al. Z Physiol Chem. 314 28 1959, IR: Koegel et al. J Am Chem Soc 77 5708 1977, Beilstein 4 IV 2501.]
Check Digit Verification of cas no
The CAS Registry Mumber 1482-97-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1482-97:
(6*1)+(5*4)+(4*8)+(3*2)+(2*9)+(1*7)=89
89 % 10 = 9
So 1482-97-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N2O2.ClH/c4-1-2(5)3(6)7;/h2H,1,4-5H2,(H,6,7);1H/t2-;/m0./s1
1482-97-9Relevant articles and documents
Synthesis of the pyrimidine moieties of bleomycin and epibleomycin
Arai,Hagmann,Suguna,Hecht
, p. 6631 - 6633 (1980)
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Tn Antigen Mimics by Ring-Opening of Chiral Cyclic Sulfamidates with Carbohydrate C1- S- and C1- O-Nucleophiles
Tovillas, Pablo,García, Iván,Oroz, Paula,Mazo, Nuria,Avenoza, Alberto,Corzana, Francisco,Jiménez-Osés, Gonzalo,Busto, Jesús H.,Peregrina, Jesús M.
, p. 4973 - 4980 (2018/05/17)
Starting from commercially available (S)-isoserine and effectively accessible (S)-α-methylserine, enantiopure cyclic sulfamidates have been prepared as chiral building blocks for the synthesis of various S- and O-glycosylated amino acid derivatives, inclu
Bacterial preparation of enantiopure unactivated aziridine-2-carboxamides and their transformation into enantiopure nonnatural amino acids and vic-diamines
Moran-Ramallal, Roberto,Liz, Ramon,Gotor, Vicente
, p. 521 - 524 (2007/10/03)
Enantiopure (1R,2S)-1-benzyl- and 1-arylaziridine-2-carboxamides were obtained by kinetic resolution of their racemates by Rhodococcus rhodochrous IFO 15564 catalyzed hydrolysis. Several regio- and enantioselective nucleophilic ring openings of (1R,2S)-1-benzylaziridine-2-carboxamide or its LAH-reduced product led to a series of enantiopure products, such as O-methyl-L-serine and some vicinal diamines.
