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1482-97-9

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1482-97-9 Usage

Chemical Properties

white crystalline powder

Uses

(2S)-2,3-Diaminopropanoic Acid Hydrochloride is a non-proteinogenic amino acid that can be used in the synthesis of peptides containing non-proteinogenic amino acids.

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

1482-97-9 Well-known Company Product Price

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  • TCI America

  • (D1377)  (S)-(+)-2,3-Diaminopropionic Acid Hydrochloride  >97.0%(T)

  • 1482-97-9

  • 100mg

  • 490.00CNY

  • Detail
  • TCI America

  • (D1377)  (S)-(+)-2,3-Diaminopropionic Acid Hydrochloride  >97.0%(T)

  • 1482-97-9

  • 1g

  • 1,990.00CNY

  • Detail

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.

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