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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)-

Galactitol, 1-deoxy-

OC[C@H]([C@@H]([C@@H]([C@@H](O)C)O)O)O Request for Quotation
Chemical Name: Galactitol, 1-deoxy-
CAS Number: 13074-06-1
Product Number: AG000UW9(AGN-PC-0O0YPS)
Synonyms:
MDL No:
Molecular Formula: C6H14O5
Molecular Weight: 166.1724

Identification/Properties

Computed Properties
Molecular Weight:
166.173g/mol
XLogP3:
-2
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
166.084g/mol
Monoisotopic Mass:
166.084g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
107
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2R,3S,4R,5S)-Hexane-1,2,3,4,5-pentaol is a versatile compound commonly utilized in chemical synthesis due to its structural properties and reactivity. In organic synthesis, this compound serves primarily as a valuable building block for the preparation of complex molecules. Its multiple hydroxyl groups enable it to participate in various reactions, such as esterification, etherification, and acetylation, leading to the formation of diverse derivatives. Additionally, the chiral nature of (2R,3S,4R,5S)-Hexane-1,2,3,4,5-pentaol makes it a crucial starting material for developing enantiomerically pure compounds, which are essential in pharmaceutical and agrochemical industries. Furthermore, its ability to act as a protecting group for alcohols allows for selective manipulations in synthesis, facilitating the construction of intricate molecular architectures. Overall, the application of (2R,3S,4R,5S)-Hexane-1,2,3,4,5-pentaol in chemical synthesis showcases its significant role in advancing the field of organic chemistry.