Isomannide
Isomannide Basic information
- Product Name:
- Isomannide
- Synonyms:
-
- 1,4:3,6-DIANHYDROMANNITOL
- ISOMANNIDE
- 1,4
- Perhydro-3,6-dihydroxyfuro[3,2-b]furan
- Keratin 5 &
- Milnacipran Impurity 14
- (3R,3aR,6R,6aR)-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan-3,6-diol
- I**isomannide、1,4:3,6-dianhydro-D-manni
- CAS:
- 641-74-7
- MF:
- C6H10O4
- MW:
- 146.14
- EINECS:
- 211-374-1
- Product Categories:
-
- Alcohols and Derivatives
- Heterocycles
- Glycon Biochem
- Mol File:
- 641-74-7.mol
Isomannide Chemical Properties
- Melting point:
- 80-85 °C (lit.)
- alpha
- 89 º (c=3, H2O)
- Boiling point:
- 150 °C / 12mmHg
- Density
- 1.0945 (rough estimate)
- refractive index
- 1.4128 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform (Slightly), Methanol (Slightly), Water
- form
- Solid
- pka
- 13.17±0.40(Predicted)
- color
- White to Off-White
- optical activity
- [α]25/D +89°, c = 3 in H2O
- Water Solubility
- almost transparency
- BRN
- 80509
- CAS DataBase Reference
- 641-74-7(CAS DataBase Reference)
MSDS
- Language:English Provider:Isomannide
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
Isomannide Usage And Synthesis
Chemical Properties
White to off-white powder
Uses
1,4:3,6-Dianhydro-D-mannitol is a reagent used in the synthesis of new isomannide-based peptidomimetic as human tissue kallikrein 1 inhibitor using Ugi multicomponent reaction. It also functions as a chiral ligand for stereoselective synthesis.
Synthesis
69-65-8
641-74-7
The general procedure for the synthesis of 1,4:3,6-bis-anhydromannitol from D-mannitol was as follows: 1350 g of crystalline D-mannitol was added to a reduced-pressure reactor equipped with a stirrer and heated to 170 °C to melt it. Subsequently, 10 g of 98% concentrated sulfuric acid was added to the melt, and the reaction lasted for 20 h at 170 °C and 2 kPa with nitrogen gas being passed at a flow rate of 200 mL/min. Upon completion of the reaction, the product was cooled to 90 °C and 30 g of 48% (w/w) aqueous sodium hydroxide solution was added to give crude 1,4:3,6-bis-anhydromannitol. Next, 39 g of horseshoe-based wood activated carbon (trade name: Tyco K, produced by Futamura Chemical Co., Ltd.) was added to the crude product and stirred for 3 h for decolorization to obtain a mixture to be distilled. Water was distilled from the mixture at 120 °C and 5 kPa. Subsequently, a reduced pressure distillation was carried out at 170 °C and 0.3 kPa under reduced pressure by passing nitrogen at a flow rate of 200 mL/min, resulting in 491 g of product. A portion of the distilled product was taken and the pH of the mixture was determined to be 10 according to the method of Example 1.
References
[1] Green Chemistry, 2015, vol. 17, # 2, p. A1176 - A1185
[2] Journal of Chemical Crystallography, 1997, vol. 27, # 3, p. 161 - 166
[3] Carbohydrate Research, 1980, vol. 79, p. 133 - 141
[4] Journal of Organometallic Chemistry, 1983, vol. 253, # 2, p. 249 - 252
[5] Journal of the American Chemical Society, 1946, vol. 68, p. 930,934
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