145124-97-6

Basic information

• Product Name: Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside
• Synonyms: Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside;Ethyl 2,3-O-isopropylidene-alpha-L-thiorhamnopyranoside;Ethyl-2,3-O-isopropylidene-a-L-thiorhamnopyranoside;Ethyl 2,3-O-isopropylidene-1-thio-α-L-rhaMnopyranoside
• CAS NO: 145124-97-6
• Molecular Formula: C₁₁H₂₀O₄S
• Molecular Weight: 248.3391
• Mol File: 145124-97-6.mol

Chemical Properties

• Boiling Point: 375.6±42.0 °C(Predicted)
• Appearance: /
• Density: 1.20±0.1 g/cm3(Predicted)
• PKA: 13.20±0.70(Predicted)
• CAS DataBase Reference: Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside(145124-97-6)
• EPA Substance Registry System: Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside(145124-97-6)

Safety Data

• Hazardous Substances Data: 145124-97-6(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside is used as a key intermediate in organic synthesis for its ability to protect the hydroxyl group of rhamnose, facilitating the creation of more complex molecules with specific functional groups.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside is used as a building block for the synthesis of drugs. Its reactivity and protective properties allow for the development of novel therapeutic agents with specific pharmacological properties.
Used in Agrochemical Industry:
Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside is also utilized in the agrochemical industry for the production of pesticides. Its chemical properties make it suitable for the synthesis of compounds that can protect crops from pests and diseases.
Used in Chemical Research:
In the realm of chemical research, Ethyl 2,3-O-isopropylidene-1-thio-a-L-rhamnopyranoside is used as a model or a reagent to study various chemical reactions and mechanisms, contributing to the advancement of organic chemistry and related fields.

Upstream product

• 145124-95-4 Ethyl 6-O-(p-toluenesulfonyl)-1-thio-α-D-mannopyranoside 
• 7473-36-1 ethyl 1-thio-α-D-mannopyranoside 
• 151669-30-6 ethyl 2,3-di-O-isopropylidene-1-thio-α-D-mannopyranoside 
• 887478-20-8 ethyl 6-deoxy-6-iodo-2,3-O-isopropylidene-1-thio-α-D-mannopyranoside 
• 145124-96-5 Ethyl 2,3-O-isopropylidene-6-O-(p-toluenesulfonyl)-1-thio-α-D-mannopyranoside 

Downstream Products

• 151669-31-7 Ethyl 4-O-benzyl-1-thio-α-D-rhamnopyranoside 
• 151669-33-9 Ethyl 3-O-acetyl-4-O-benzyl-2-O-methyl-1-thio-α-D-rhamnopyranoside 
• 213386-06-2 Ethyl 4-O-benzyl-2-O-methyl-1-thio-α-D-rhamnopyranoside 
• 176039-82-0 ethyl 3-O-benzyl-2-O-chloroacetyl-4-O-methyl-1-thio-α-D-rhamnopyranoside 
• 176039-81-9 ethyl 3-O-benzyl-4-O-methyl-1-thio-α-D-rhamnopyranoside 
• 176039-88-6 4-[2-(benzyloxycarbonylamino)ethyl]phenyl 2,4-di-O-methyl-3-O-{4-O-benzyl-2-O-methyl-3-O-[4-O-acetyl-2-O-methyl-3-O-(3-O-benzyl-2-O-chloroacetyl-4-O-methyl-α-D-rhamnopyranoside)-α-L-fucopyranosyl]-α-L-rhamnopyranosyl}-α-L-rhamnopyranoside 
• 176039-89-7 4-[2-(benzyloxycarbonylamino)ethyl]phenyl 2,4-di-O-methyl-3-O-{4-O-benzyl-2-O-methyl-3-O-[4-O-acetyl-2-O-methyl-3-O-(3-O-benzyl-4-O-methyl-α-D-rhamnopyranoside)-α-L-fucopyranosyl]-α-L-rhamnopyranosyl}-α-L-rhamnopyranoside 

Relevant articles and documents

Synthesis of tetrasaccharide repeating unit of the O-antigen from enterohemorrhagic Escherichia coli O157 in the form of its 2-(trimethylsilyl) ethyl glycoside

Two α-linked disaccharide derivatives, ethyl 3,4,6-tri-O-acetyl-2- azido-2-deoxy-α-D-galactopyranosyl-(1 → 2)-4-azido-3-O-benzyl-4,6- dideoxy-1-thio-α-D-mannopyranoside (10) and 2-(trimethylsilyl)ethyl 3-O-acetyl-4-O-benzoyl-2-O-benzyl-α-L-fucopyranosyl-(

Synthesis of p-trifluoroacetamidophenyl 6-deoxy-2-O--α-L-rhamnopyranosyl>-α-L-talopyranoside: a spacer armed tetrasaccharide glycopeptidolipid antigen of Mycobacterium avium serovar 2

The synthesis of the title tetrasaccharide glycoside 38 is reported. p-Nitrophenyl endo-3,4-O-benzylidene-6-deoxy-α-L-talopyranoside (4), 3-O-acetyl-2,4-di-O-benzyl-α-L-rhamnopyranosyl trichloroacetimidate (7), methyl 3-O-acetyl-4-O-benzyl-2-O-methyl-1-th