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2-Deoxy-D-galactose - 98%, high purity , CAS No.1949-89-9
Basic Description
Synonyms
2-Deoxy-D-galactose | 2-deoxy-D-lyxo-hexose | 531K2IOK5Q | EINECS 217-765-3 | SCHEMBL148114 | (+)-2-DEOXY-D-GALACTOSE | lyxo-Hexose, 2-deoxy- | (3R,4R,5R)-3,4,5,6-tetrahydroxyhexanal | DTXSID30985215 | CHEBI:27411 | DTXSID9075163 | 2-Deoxygalactose | D-ly
Specifications & Purity
≥98%
Storage Temp
Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
Hexose analog that can be incorporated into rat gangliosides GM2 and GD3 in positions normally occupied by galactose. 2-Deoxy-D-galactose has been suggested to act as an inhibitor of fucosylation. It has also been used for competitive elution of Anadarin P lectin (a galactosyl-binding lectin from blood clam).
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Fatty Acyls
Subclass
Fatty alcohols
Intermediate Tree Nodes
Not available
Direct Parent
Fatty alcohols
Alternative Parents
Medium-chain aldehydes Beta-hydroxy aldehydes Alpha-hydrogen aldehydes Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic acyclic compounds
Substituents
Fatty alcohol - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydrogen aldehyde - Secondary alcohol - Polyol - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
External Descriptors
deoxygalactose
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
IUPAC Name
(3R,4R,5R)-3,4,5,6-tetrahydroxyhexanal
INCHI
InChI=1S/C6H12O5/c7-2-1-4(9)6(11)5(10)3-8/h2,4-6,8-11H,1,3H2/t4-,5-,6-/m1/s1
InChIKey
VRYALKFFQXWPIH-HSUXUTPPSA-N
Smiles
C(C=O)C(C(C(CO)O)O)O
Isomeric SMILES
C(C=O)[C@H]([C@H]([C@@H](CO)O)O)O
WGK Germany
3
Molecular Weight
164.16
Beilstein
1723333
Reaxy-Rn
2041872
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2041872&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water.
Sensitivity
Moisture Sensitive
Specific Rotation[α]
60°
Melt Point(°C)
107-110°C
Molecular Weight
164.160 g/mol
XLogP3
-2.900
Hydrogen Bond Donor Count
4
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
5
Exact Mass
164.068 Da
Monoisotopic Mass
164.068 Da
Topological Polar Surface Area
98.000 Ų
Heavy Atom Count
11
Formal Charge
0
Complexity
116.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
3
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
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