CAS 141846-57-3

α-L-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-methylbenzoate)

Description:

α-L-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-methylbenzoate) is a synthetic organic compound characterized by its furanose sugar structure, which is a five-membered ring containing oxygen. This compound features a chloride substituent, indicating its potential reactivity in nucleophilic substitution reactions. The presence of two 4-methylbenzoate ester groups suggests that it may exhibit hydrophobic properties, which can influence its solubility and interaction with biological membranes. The 2-deoxy configuration indicates the absence of a hydroxyl group at the second carbon, which is significant in biological contexts, particularly in nucleoside chemistry. This compound may be of interest in medicinal chemistry and biochemistry, particularly for its potential applications in the synthesis of nucleoside analogs or as a building block in the development of glycosylated compounds. Its specific reactivity and stability would depend on the surrounding conditions, such as pH and solvent, making it a versatile candidate for further chemical modifications.

Formula: C₂₁H₂₁ClO₅

InChI: InChI=1S/C21H21ClO5/c1-13-3-7-15(8-4-13)20(23)25-12-18-17(11-19(22)26-18)27-21(24)16-9-5-14(2)6-10-16/h3-10,17-19H,11-12H2,1-2H3/t17-,18+,19-/m1/s1

InChI key: InChIKey=FJHSYOMVMMNQJQ-CEXWTWQISA-N

SMILES: C(OC(=O)C1=CC=C(C)C=C1)[C@H]2[C@H](OC(=O)C3=CC=C(C)C=C3)C[C@H](Cl)O2

Synonyms:

• 1-Chloro-2-deoxy-3,5-di-O-toluoyl-L-ribose
• 1-Chloro-3,5-di-O-toluoyl-2-deoxy-L-ribofuranose
• 2-Deoxy-3,5-di-O-p-toluoyl-α-L-ribofuranosyl Chloride
• 2-Deoxy-α-L-erythro-pentofuranosyl Chloride 3,5-Bis(4-methylbenzoate)
• 3,5-Di-O-(4-methylbenzoyl)-2-deoxy-α-<span class="text-smallcaps">L</span>-erythro-pentofuranosyl chloride
• Chloro-3,5-di-O-toluoyl-2-deoxy-α-L-ribofuranose
• α-<span class="text-smallcaps">L</span>-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-methylbenzoate)
• α-<span class="text-smallcaps">L</span>-erythro-Pentofuranosyl chloride, 2-deoxy-, bis(4-methylbenzoate)
• α-L-erythro-Pentofuranosyl chloride, 2-deoxy-, bis(4-methylbenzoate)
• α-L-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-methylbenzoate)
• 3,5-Di-O-(4-methylbenzoyl)-2-deoxy-α-L-erythro-pentofuranosyl chloride

(2S,3R,5R)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate

CAS: 141846-57-3

Formula: C₂₁H₂₁ClO₅

Purity: 90%

Color and Shape: Solid

Molecular weight: 388.8414

Ref: IN-DA006WXD

(2S,3R,5R)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate

CAS: 141846-57-3

(2S,3R,5R)-5-Chloro-2-(((4-methylbenzoyl)oxy)methyl)tetrahydrofuran-3-yl 4-methylbenzoate

Purity: 90%

Molecular weight: 388.85g/mol

Ref: 54-OR1065207

2-Deoxy-3,5-di-O-p-toluoyl-α-L-ribofuranosyl chloride

CAS: 141846-57-3

Molecular weight: 388.84

Ref: 7W-GC5142

Telbivudine Impurity 3

CAS: 141846-57-3

Formula: C₂₁H₂₁ClO₅

Molecular weight: 388.84

Ref: 4Z-T-255

1-Chloro-2-deoxy-3,5-di-O-toluoyl-L-ribofuranose

CAS: 141846-57-3

1-Chloro-2-deoxy-3,5-di-O-toluoyl-L-ribofuranose is a synthetic glycosylation agent with high purity and custom synthesis. It is a monosaccharide that can be used for the modification of complex carbohydrates, such as saccharides and polysaccharides. 1-Chloro-2-deoxyribofuranose is also known to react with other types of sugars to form glycosylated products. This product can be fluorinated or methylated to create new derivatives.

Formula: C₂₁H₂₁ClO₅

Purity: (Argentometric Titration) Min 90%

Color and Shape: Powder

Molecular weight: 388.84 g/mol

Ref: 3D-MC04436

2-Deoxy-3,5-di-O-p-toluoyl-a-L-ribofuranosyl Chloride

CAS: 141846-57-3

Stability Moisture Sensitive, Unstable in Solution
Applications 2-Deoxy-3,5-di-O-p-toluoyl-α-L-ribofuranosyl Chloride (cas# 141846-57-3) is a compound useful in organic synthesis.

Formula: C₂₁H₂₁ClO₅

Color and Shape: Neat

Molecular weight: 388.84

Ref: TR-D232870