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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

D-Streptamine,2-deoxy-4-O-(2,6-diamino-2,6-dideoxy-a-D-glucopyranosyl)-,tetrahydrochloride

NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@H]([C@@H]([C@H]2O)O)N)[C@@H]([C@H]([C@@H]1O)O)N.Cl.Cl.Cl.Cl Request for Quotation
Chemical Name: D-Streptamine,2-deoxy-4-O-(2,6-diamino-2,6-dideoxy-a-D-glucopyranosyl)-,tetrahydrochloride
CAS Number: 15446-43-2
Product Number: AG00ADHY(AGN-PC-0Q6Q3H)
Synonyms:
MDL No: MFCD08703164
Molecular Formula: C12H30Cl4N4O6
Molecular Weight: 468.2018

Identification/Properties

Computed Properties
Molecular Weight:
468.194g/mol
Hydrogen Bond Donor Count:
12
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
3
Exact Mass:
468.089g/mol
Monoisotopic Mass:
466.092g/mol
Topological Polar Surface Area:
204A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
378
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
10
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
5
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,3S,4R,5R,6R)-5-Amino-2-(aminomethyl)-6-{[(1R,2R,3S,4R,6S)-4,6-diamino-2,3-dihydroxycyclohexyl]oxy}oxane-3,4-diol tetrahydrochloride serves as a versatile building block in chemical synthesis. Its unique structure, containing multiple amine and hydroxyl functional groups, makes it valuable for creating complex molecules through various chemical reactions. In synthesis, this compound can be utilized as a chiral starting material for the construction of biologically active compounds, pharmaceutical intermediates, or novel materials. Its distinct stereochemistry and functional groups offer opportunities for forming specific bonds and molecular arrangements, enabling chemists to design and prepare diverse compounds with desired properties.