CAS 4306-35-8
:1,2-O-(1-Methylethylidene)-D-mannitol
Description:
1,2-O-(1-Methylethylidene)-D-mannitol, with the CAS number 4306-35-8, is a chemical compound derived from D-mannitol, a sugar alcohol. This compound features a methylethylidene group that modifies the hydroxyl groups on the mannitol structure, influencing its chemical properties and reactivity. It is typically characterized by its white crystalline appearance and is soluble in water, which is a common trait among sugar alcohols. The presence of the methylethylidene group can enhance its stability and alter its interaction with biological systems, making it of interest in various applications, including pharmaceuticals and food science. Additionally, the compound may exhibit specific optical activity due to its chiral centers, which is a significant characteristic in the study of carbohydrates and their derivatives. Overall, 1,2-O-(1-Methylethylidene)-D-mannitol represents a unique modification of mannitol that could have implications in both industrial and research settings.
Formula:C9H18O6
InChI:InChI=1S/C9H18O6/c1-9(2)14-4-6(15-9)8(13)7(12)5(11)3-10/h5-8,10-13H,3-4H2,1-2H3/t5-,6-,7-,8-/m1/s1
InChI key:InChIKey=CWNIYRGNKYHYHW-WCTZXXKLSA-N
SMILES:[C@@H]([C@@H]([C@@H](CO)O)O)(O)[C@@]1(OC(C)(C)OC1)[H]
Synonyms:- 1,2-O-(1-Methylethylidene)-<span class="text-smallcaps">D</span>-mannitol
- 1,2-O-(1-methylethylidene)hexitol
- <span class="text-smallcaps">D</span>-Mannitol, 1,2-O-(1-methylethylidene)-
- Mannitol, 1,2-O-isopropylidene-
- Mannitol, 1,2-O-isopropylidene-, <span class="text-smallcaps">D</span>-
- NSC 226057
- 1,2-O-(1-Methylethylidene)-D-mannitol
- Mannitol, 1,2-O-isopropylidene-, D-
- D-Mannitol, 1,2-O-(1-methylethylidene)-
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Found 3 products.
1,2-O-Isopropylidene-D-mannitol
CAS:1,2-O-Isopropylidene-D-mannitolColor and Shape:SolidMolecular weight:222.24g/mol1,2-O-Isopropylidene-D-mannitol
CAS:<p>1,2-O-Isopropylidene-D-mannitol is an alditol that is synthesized by the reaction of 1,2-O-isopropylidene glycerol with sodium sulfide. This product can be further reacted with allylamine to form a thiepane derivative. Thiepane derivatives are polyhydroxylated and have been shown to have antibacterial activity against Staphylococcus aureus, Mycobacterium tuberculosis, and Streptococcus pneumoniae.</p>Formula:C9H18O6Purity:Min. 95%Color and Shape:PowderMolecular weight:222.24 g/mol


