ChemicalBook Product Catalog Organic Chemistry Nitrile compound N-METHYL-1-DEOXYNOJIRIMYCIN

N-METHYL-1-DEOXYNOJIRIMYCIN

N-METHYL-1-DEOXYNOJIRIMYCIN Basic information
Product Name:N-METHYL-1-DEOXYNOJIRIMYCIN
Synonyms:1,5-DIDEOXY-1,5-IMINO-1-METHYL-D-SORBITOL;N-METHYL-1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL;N-METHYL-1-DEOXYNOJIRIMYCIN;N-METHYLDEOXYNOJIRIMYCIN;DEOXYNOJIRIMYCIN, N-METHYL-;(2R)-1-Methyl-2α-(hydroxymethyl)-3β,4α,5β-piperidinetriol;(2R)-2α-(Hydroxymethyl)-1-methyl-3β,4α,5β-piperidinetriol;MOR-14
CAS:69567-10-8
MF:C7H15NO4
MW:177.2
EINECS:203-703-2
Product Categories:13C & 2H Sugars;Carbohydrates & Derivatives;Glycosidase Inhibitors;Inhibitors
Mol File:69567-10-8.mol
N-METHYL-1-DEOXYNOJIRIMYCIN Structure
N-METHYL-1-DEOXYNOJIRIMYCIN Chemical Properties
Melting point 126-128°C
Boiling point 367.2±42.0 °C(Predicted)
density 1.394±0.06 g/cm3(Predicted)
storage temp. 2-8°C
solubility Methanol (Slightly, Sonicated), Water (Slightly)
pka13.71±0.70(Predicted)
form Solid
color White to Off-White
BRN 1524564
Stability:Hygroscopic
Safety Information
Safety Statements 22-24/25
WGK Germany 3
F 10
HS Code 2933999700
MSDS Information
ProviderLanguage
SigmaAldrich English
N-METHYL-1-DEOXYNOJIRIMYCIN Usage And Synthesis
Chemical PropertiesWhite to Off-White
UsesInterfers with the normal processing of N-linked glycoproteins by inhibiting the action of glucosidases that remove glycosyl residues from Glc3Man9GlcNAc2 following the addition of this moiety to a nascent polypeptide.
General DescriptionChemical structure: glucosamine
Biochem/physiol ActionsInterferes with metabolism of N-linked glycoproteins by inhibition of glucosidase.
N-METHYL-1-DEOXYNOJIRIMYCIN Preparation Products And Raw materials
N-(7-Oxa-9,9,9-trifluorononyl)deoxynojirimycin 4,6-O-Benzylidene-N-Boc-1,5-imino-D-glucitol N-BUTYLDEOXYNOJIRIMYCIN CAMIGLIBOSE Miglitol N-(7-Oxadecyl)deoxynojirimycin N-Dodecyldeoxynojirimycin N-(n-Nonyl)deoxynojirimycin N-5-Carboxypentyl-1-deoxynojirimycin N-(5-ADAMANTANE-1-YL-METHOXY)-PENTYL-DEOXYNOJIRIMYCIN glycovir 4,6-O-BENZYLIDENE-N-(TERT-BUTOXYCARBONYL)-2-O-(4-TOLUENESULFONYL)-1,5-IMINO-D-GLUCITOL N-BUTYLDEOXYNOJIRIMYCIN, HYDROCHLORIDE 1,5-dideoxy-1,5-[[2-[4-(ethoxycarbonyl)phenoxy]ethyl]imino]-D-glucitol N-METHYL-1-DEOXYNOJIRIMYCIN TETRA-O-BENZYL-N-(HYDROXYETHYL)-1-DESOXYNOJIRIMICIN N-Boc-1,5-imino-1,5-dideoxy-D-glucitol N-ETHYLDEOXYNOJIRIMYCIN, HYDROCHLORIDE
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