Threitol

Threitol^[1]
Names

Systematic IUPAC name (2R,3R)-Butane-1,2,3,4-tetrol
Other names (2R,3R)-Butane-1,2,3,4-tetraol (not recommended)
Identifiers
CAS Number	7493-90-5 (DL)^N
3D model (Jmol)	Interactive image
ChEBI	CHEBI:48300^Y
ChemSpider	147828^Y
ECHA InfoCard	100.150.149
KEGG	C16884^Y
PubChem	169019
UNII	6DN82XBT5M^N
InChI InChI=1S/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2/t3-,4-/m1/s1^Y Key: UNXHWFMMPAWVPI-QWWZWVQMSA-N^Y InChI=1/C4H10O4/c5-1-3(7)4(8)2-6/h3-8H,1-2H2/t3-,4-/m1/s1 Key: UNXHWFMMPAWVPI-QWWZWVQMBP
SMILES OC[C@@H](O)[C@H](O)CO
Properties
Chemical formula	C₄H₁₀O₄
Molar mass	122.12
Appearance	Solid
Melting point	88 to 90 °C (190 to 194 °F; 361 to 363 K)
Hazards
R-phrases	R36/37/38
S-phrases	S26 S36
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

Threitol is a four-carbon sugar alcohol with the molecular formula C₄H₁₀O₄. It is primarily used as an intermediate in the chemical synthesis of other compounds. It is the diastereomer of Erythritol.

Threitol is found in the edible fungus Armillaria mellea.^[2]

Threitol is used in the synthesis of Treosulfan.

References

↑ Threitol at Sigma-Alrich
↑ Elks, J.; Ganellin, C. R. (1990). doi:10.1007/978-1-4757-2085-3. Missing or empty |title= (help)

Sugar alcohols

2-carbon	Ethylene glycol

3-carbon	Glycerol

4-carbon	Erythritol Threitol

5-carbon	Arabitol Ribitol Xylitol

6-carbon	Mannitol Sorbitol Galactitol Iditol

7-carbon	Volemitol

Deoxy sugar alcohols	Fucitol

Cyclic sugar alcohols	Inositol

Glycylglycitols	Maltitol Lactitol Isomalt Maltotriitol Maltotetraitol Polyglycitol

This article is issued from Wikipedia - version of the 10/11/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.

Threitol

See also

References