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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)-

a-D-Mannopyranosyl chloride, tetraacetate

CC(=O)OC[C@H]1O[C@H](Cl)[C@H]([C@H]([C@@H]1OC(=O)C)OC(=O)C)OC(=O)C Request for Quotation
Chemical Name: a-D-Mannopyranosyl chloride, tetraacetate
CAS Number: 14257-40-0
Product Number: AG007ZD4(AGN-PC-0PSKRC)
Synonyms:
MDL No: MFCD00067355
Molecular Formula: C14H19ClO9
Molecular Weight: 366.7483

Identification/Properties

Computed Properties
Molecular Weight:
366.747g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
9
Exact Mass:
366.072g/mol
Monoisotopic Mass:
366.072g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
507
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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


The compound (2S,3S,4S,5S)-6-Chloro-2,3,4,5-tetrahydroxyhexanal, commonly referred to as $name$, plays a crucial role in chemical synthesis due to its unique stereochemical properties. It serves as a versatile building block in organic chemistry, particularly in the synthesis of complex molecules and pharmaceutical intermediates. $name$ can be used as a chiral starting material for the preparation of various natural products and pharmaceuticals. Its specific stereochemistry allows for the creation of enantiomerically pure compounds, which are essential in drug development and medicinal chemistry. Additionally, $name$ can participate in a range of chemical reactions, including nucleophilic substitutions, acylations, and condensations, making it a valuable reagent in organic synthesis. Its chlorine atom and multiple hydroxyl groups provide opportunities for functional group transformations, enabling chemists to introduce diverse substituents and modify molecular structures effectively.Overall, the application of (2S,3S,4S,5S)-6-Chloro-2,3,4,5-tetrahydroxyhexanal in chemical synthesis is instrumental in the creation of complex molecules with precise stereochemistry, making it an indispensable tool for synthetic chemists.