CAS 4990-82-3

methyl 4,6-dichloro-4,6-dideoxy-alpha-D-galactopyranoside

Description:

Methyl 4,6-dichloro-4,6-dideoxy-alpha-D-galactopyranoside is a synthetic carbohydrate derivative characterized by the presence of two chlorine atoms at the 4 and 6 positions of the galactopyranoside structure, along with a methyl ester group. This compound is a modified sugar, which can exhibit unique biochemical properties due to the halogen substitutions, potentially influencing its reactivity and interactions with biological molecules. The presence of the methyl group enhances its lipophilicity, which may affect its solubility and permeability in biological systems. As a dideoxy sugar, it lacks hydroxyl groups at the 4 and 6 positions, which can significantly alter its biological activity compared to its parent sugar. This compound may be of interest in research related to glycoscience, medicinal chemistry, or as a potential building block in the synthesis of more complex carbohydrate structures. Its CAS number, 4990-82-3, allows for easy identification in chemical databases and literature.

Formula: C₇H₁₂Cl₂O₄

InChI: InChI=1/C7H12Cl2O4/c1-12-7-6(11)5(10)4(9)3(2-8)13-7/h3-7,10-11H,2H2,1H3/t3-,4+,5+,6-,7+/m1/s1

Synonyms:

• alpha-D-galactopyranoside, methyl 4,6-dichloro-4,6-dideoxy-
• Methyl 4,6-dichloro-4,6-dideoxy-alpha-D-galactopyranoside

Methyl 4,6-dichloro-4,6-dideoxy-α-D-galactopyranoside

CAS: 4990-82-3

Methyl 4,6-dichloro-4,6-dideoxy-α-D-galactopyranoside

Purity: >98%

Molecular weight: 231.07g/mol

Ref: 54-BICL4283

Methyl 4,6-dichloro-4,6-dideoxy-α-D-galactopyranoside

CAS: 4990-82-3

Ref: 7W-GC5419

Methyl 4,6-dichloro-4,6-dideoxy-a-D-galactopyranoside

CAS: 4990-82-3

Methyl 4,6-dichloro-4,6-dideoxy-a-D-galactopyranoside is an innovative sweetener that can be used in food and drinks. It is a type of sugar alcohol with a sweet taste similar to sucrose. This substance is not metabolized by bacteria in the intestine or absorbed into the bloodstream. Methyl 4,6-dichloro-4,6-dideoxy-a-D-galactopyranoside has been shown to inhibit the activity of nerve cells by preventing the release of neurotransmitters such as glutamate and GABA. This inhibition mechanism is thought to be due to its ability to enhance the release of chloride ions from nerve cells. The model Euclidean was used to predict the potential stimulatory effect on tympanic membrane (eardrum) cells when exposed to methyl 4,6-dichloro-4,6-dideoxy-a-D

Formula: C₇H₁₂Cl₂O₄

Purity: Min. 95%

Molecular weight: 231.08 g/mol

Ref: 3D-MM08882