CAS 74410-48-3
:1-Deoxy-1-[(phenylmethyl)amino]-D-glucitol
Description:
1-Deoxy-1-[(phenylmethyl)amino]-D-glucitol, with the CAS number 74410-48-3, is a chemical compound that belongs to the class of amino sugars. It is characterized by the presence of a glucitol backbone, which is a derivative of glucose, modified by the substitution of a phenylmethyl (benzyl) amino group at the first carbon position. This modification imparts unique properties to the molecule, influencing its solubility, reactivity, and potential biological activity. The compound is typically a white to off-white solid and is soluble in polar solvents, such as water and alcohols, due to the hydroxyl groups present in its structure. Its amino group can participate in various chemical reactions, making it a candidate for applications in medicinal chemistry and biochemistry. Additionally, the presence of the phenylmethyl group may enhance its interaction with biological targets, potentially influencing its pharmacological properties. Overall, 1-Deoxy-1-[(phenylmethyl)amino]-D-glucitol is of interest for research in glycoscience and drug development.
Formula:C13H21NO5
InChI:InChI=1S/C13H21NO5/c15-8-11(17)13(19)12(18)10(16)7-14-6-9-4-2-1-3-5-9/h1-5,10-19H,6-8H2/t10-,11+,12+,13+/m0/s1
InChI key:InChIKey=GXNAHMSFQNFFSO-UMSGYPCISA-N
SMILES:C(NC[C@@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O)C1=CC=CC=C1
Synonyms:- 1-Deoxy-1-[(phenylmethyl)amino]-<span class="text-smallcaps">D</span>-glucitol
- <span class="text-smallcaps">D</span>-Glucitol, 1-deoxy-1-[(phenylmethyl)amino]-
- Sorbitol, 1-benzylamino-1-deoxy-
- Sorbitol,1-benzylamino-1-deoxy- (6CI)
- D-Glucitol, 1-deoxy-1-[(phenylmethyl)amino]-
- 1-Deoxy-1-[(phenylmethyl)amino]-D-glucitol
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Found 1 products.
N-Benzyl-D-glucamine
CAS:<p>N-Benzyl-D-glucamine is a metal chelate that binds to lead and other heavy metals. It is used as a transport inhibitor for the elimination of lead from the body. N-Benzyl-D-glucamine has been shown to be effective in lowering blood levels of lead, with an elimination rate of 50% within 4 hours. When administered orally, this drug also has inhibitory effects on the absorption of lead from gastrointestinal tissues, which may be due to its inhibition of urea nitrogen and gastrointestinal toxicities. This drug can also reduce the excretion of cadmium and aromatic hydrocarbons in urine samples.</p>Purity:Min. 95%
