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551942-41-7

D-glycero-D-galacto-Non-2-enonic acid,5-(acetylamino)-4-[(aminoiminomethyl)amino]-2,6-anhydro-3,4,5-trideoxy-, hydrate

Catalog#: AR00DG83  |   CAS#: 551942-41-7  |   MDL#: MFCD00866966  |   MF: C12H22N4O8  |   MW: 350.3251

Packsize Purity Price Availability Quantity
10mg 98% $24.00 Global Stock Buy Now Add To Cart
50mg 98% $88.00 Global Stock Buy Now Add To Cart
100mg 98% $141.00 Global Stock Buy Now Add To Cart
250mg 98% $274.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DG83
Chemical Name D-glycero-D-galacto-Non-2-enonic acid,5-(acetylamino)-4-[(aminoiminomethyl)amino]-2,6-anhydro-3,4,5-trideoxy-, hydrate
CAS Number 551942-41-7
Molecular Formula C12H22N4O8
Molecular Weight 350.3251
MDL Number MFCD00866966
SMILES OCC(C(C1OC(=CC(C1NC(=O)C)N=C(N)N)C(=O)O)O)O.O

(2R,3R,4S)-3-Acetamido-2-((1R,2R)-1,3-dihydroxy-2-methylpropyl)-4-guanidino-3,4-dihydro-2H-pyran-6-carboxylic acid hydrate (1:x) is a versatile compound that finds crucial applications in chemical synthesis. This compound serves as a key reactant in the formation of various complex molecules through a series of chemical reactions. Its unique structure and functional groups make it an essential building block for the creation of novel compounds in the laboratory setting.In chemical synthesis, (2R,3R,4S)-3-Acetamido-2-((1R,2R)-1,3-dihydroxy-2-methylpropyl)-4-guanidino-3,4-dihydro-2H-pyran-6-carboxylic acid hydrate (1:x) can act as a nucleophile or a catalyst, participating in reactions that lead to the formation of peptide bonds, heterocycles, and other molecular structures. Its guanidino group can facilitate interactions with other molecules, allowing for the selective modification of specific functional groups within a target compound.Furthermore, the presence of the acetamido and carboxylic acid moieties in this compound provides opportunities for derivatization and further functionalization, enabling chemists to tailor the properties of the resulting molecules for specific applications. By incorporating (2R,3R,4S)-3-Acetamido-2-((1R,2R)-1,3-dihydroxy-2-methylpropyl)-4-guanidino-3,4-dihydro-2H-pyran-6-carboxylic acid hydrate (1:x) into synthetic pathways, researchers can access a wide range of chemical space and design molecules with desired biological activities or material properties.Overall, this compound plays a crucial role in advancing chemical synthesis by enabling the construction of complex molecules with precision and efficiency, making it a valuable asset in the toolkit of synthetic chemists.
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