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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)-

Butanal, 2,3,4-trihydroxy-, (2S,3S)-

OC[C@@H]([C@@H](C=O)O)O Request for Quotation
Chemical Name: Butanal, 2,3,4-trihydroxy-, (2S,3S)-
CAS Number: 533-49-3
Product Number: AG00I9IK(AGN-PC-0OBVAO)
Synonyms:
MDL No:
Molecular Formula: C4H8O4
Molecular Weight: 120.1039

Identification/Properties

Properties
MP:
164 °C
BP:
311.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
120.104g/mol
XLogP3:
-2.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
120.042g/mol
Monoisotopic Mass:
120.042g/mol
Topological Polar Surface Area:
77.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
72.4
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2S,3S)-2,3,4-Trihydroxybutanal, a compound that belongs to the class of aldehydes, plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and properties, this compound is widely utilized in organic chemistry for the creation of various complex molecules. In synthesis, (2S,3S)-2,3,4-Trihydroxybutanal serves as a key intermediate in the formation of more advanced compounds due to its ability to undergo a range of chemical reactions, including aldol condensation, oxidation, and reduction. Its hydroxy functional groups enable selective derivatization and facilitate the attachment of different substituents, making it a valuable tool for building molecular complexity in a controlled manner. This compound's significance in chemical synthesis lies in its potential to be transformed into a diverse array of products with specific functionalities, making it an indispensable component in the toolbox of synthetic chemists.