Quebrachitol

quebrachitol
IUPAC name (1R,2S,4S,5R)-6-methoxycyclohexane-1,2,3,4,5-pentol
Other names Quebrachitol L-Quebrachitol (-)-Quebrachitol 2-O-methyl-l-inositol 2-0-methyl-chiro-inositol
Identifiers
CAS number	642-38-6 Y=
PubChem	151108
ChemSpider	10254652 N
ChEMBL	CHEMBL501109 N
Jmol-3D images	Image 1
SMILES COC1C(C(C(C(C1O)O)O)O)O
InChI InChI=1S/C7H14O6/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h2-12H,1H3/t2-,3-,4-,5+,6+,7-/m0/s1 N Key: DSCFFEYYQKSRSV-FIZWYUIZSA-N N
Properties
Molecular formula	C7H14O6
Molar mass	194.18 g/mol
Exact mass	194.079038 u
Appearance	White to off-white powder
Melting point	190 - 198 °C
Solubility in water	Soluble in DMSO, dimethyl formamide, or water
N (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Quebrachitol is a naturally occurring optically active cyclitol, a cyclic polyol. It can be found in Allophylus edulis^[1] and in the serum left after the coagulation of the Hevea brasiliensis latex.^[2] It is also found in Cannabis sativa^[3] and in seabuckthorn.^[4]

It was first isolated by Tanret in 1887 from the bark of Aspidosperma quebracho. The substance was tested as a sweetening agent for diabetics in 1933. It shows a sweetening property half of that of sucrose but induces colic or diarrhoea at concentration used to render the food palatable.^[5]

Quebrachitol is a versatile building block in the construction of naturally occurring bioactive materials.^[6] For example, its conversion into antifungal (E)-β-methoxyacrylate, oudemansin X has been made.^[7]

References

1. ^ First record of l-quebrachitol in Allophylus edulis (Sapindaceae). Martina Díaz, Andrés González, Ian Castro-Gamboa, David Gonzalez and Carmen Rossini, Carbohydrate Research, Volume 343, Issue 15, 13 October 2008, Pages 2699-2700, doi:10.1016/j.carres.2008.07.014
2. ^ Quebrachitol. Jan van Alphen, Ind. Eng. Chem., 1951, 43 (1), pp 141–145, DOI: 10.1021/ie50493a041
3. ^ 1955 - ACTA UNIVERSITATIS PALACKIANAE OLOMUCENSIS - TOM. VI. - HEMP AS A MEDICAMENT, Properties of isolated substances. Prof. Jan Kabelik, A brief survey of the methods of isolation and the physical and chemical properties and structures of the isolated antibacterial substances. F. Santavy & Z. Krejci
4. ^ Some new data about antiviral and related activities of seabuckthorn principals and the prospects of their use. Shipulina L.D., All-Russian Research Institute of Medicinal and Aromatic Plants, Moscow, Russia
5. ^ An investigation of quebrachitol as a sweetening agent for diabetics. Robert Alexander McCance and Robert Daniel Lawrence, Biochem J. 1933; 27(4): 986–989
6. ^ Quebrachitol: A Versatile Building Block in the Construction of Naturally Occurring Bioactive Materials. James J. Kiddle, Chem. Rev., 1995, 95 (6), pp 2189–2202, DOI: 10.1021/cr00038a016
7. ^ Total synthesis of antibiotic (−)-oudemansin X utilizing L-quebrachitol as a chiral pool. Chida N., Yamada K. and Ogawa S., Chemistry Letters, 1992, no4, pp. 687-690

External links

• Quebrachitol on the Sigma-Aldrich website