Welcome: Chemsynlab ,carbohydrate chemistry
Language: Chinese ∷  English

61145-33-3, Cyanomethyl 2,3,4,6-tetra-O-acetyl-1-thio-beta-D-galactopyranoside,CAS:61145-33-3

61145-33-3, Cyanomethyl 2,3,4,6-tetra-O-acetyl-1-thio-beta-D-galactopyranoside,
CAS:61145-33-3
C16H21NO9S / 403.41

Cyanomethyl 2,3,4,6-tetra-O-acetyl-b-D-thiogalactopyranoside

氰基甲基 2,3,4,6-O-四乙酰基-beta-D-硫代吡喃半乳糖苷,

Cyanomethyl 2,3,4,6-tetra-O-acetyl-1-thio-beta-D-galactopyranoside (CTAG) is a chemical compound that has the potential to be used in various fields of research and industry. CTAG is a carbohydrate derivative that has a unique chemical structure, making it an attractive compound for many applications. This paper aims to provide an in-depth analysis of CTAG, including its definition and background, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, and limitations and future directions.

Definition and Background:

CTAG is a carbohydrate derivative that has a unique chemical structure. It is a thiomethylated tetrasaccharide that contains sulfur at the 1-position and a cyano group at the 6-position of the galactose unit. CTAG is commonly used as a substrate for a variety of enzymatic assays and has proved to be useful in the synthesis of other complex oligosaccharides. Overall, CTAG serves as an important synthetic intermediate for a variety of biological and industrial applications.

Synthesis and Characterization:

CTAG can be synthesized through the condensation of a lactose derivative and an S-protected thioglycoside derivative. The resulting product can be purified using silica gel column chromatography or HPLC. CTAG can be characterized using a variety of analytical techniques, including NMR spectroscopy, mass spectrometry, and HPLC.

Analytical Methods:

Analytical methods for the detection of CTAG include HPLC, NMR, and mass spectrometry. HPLC is commonly used to purify CTAG, while NMR and mass spectrometry are employed to confirm the identity and structure of CTAG.

Biological Properties:

CTAG has been shown to exhibit a range of biological properties. It can be used as a substrate for a variety of enzymes, including glycosyltransferases, lyases, and hydrolases. CTAG has also been shown to have antitumor and antimicrobial activity.

Toxicity and Safety in Scientific Experiments:

CTAG has been shown to exhibit low toxicity in scientific experiments. No adverse effects have been reported in animals or humans exposed to CTAG at concentrations used in scientific experiments.

Applications in Scientific Experiments:

CTAG is commonly used as a substrate for a variety of enzymatic assays and has been shown to have a range of antitumor and antimicrobial properties. CTAG is also an important intermediate in the synthesis of other complex oligosaccharides and has been used in the development of vaccines.

Current State of Research:

Research on CTAG is ongoing, with new applications and potential uses being discovered regularly. The unique structure and properties of CTAG make it a promising candidate for a variety of scientific applications.

Potential Implications in Various Fields of Research and Industry:

CTAG has potential applications in a variety of fields, including medicinal chemistry, enzymology, and vaccine development. The compound is also being evaluated for its potential use in agriculture, as a plant growth regulator.

Limitations and Future Directions:

While CTAG has shown great promise in a variety of scientific applications, there are limitations to its use. More research is needed to fully understand the compound's properties and potential uses. In the future, it is possible that CTAG may be modified to improve its properties or be used in conjunction with other compounds to create new and exciting applications.

Future Directions:

1. Investigation of the use of CTAG in the development of new antibiotics.

2. Study of the use of CTAG in the production of vaccines.

3. Use of CTAG to develop new methods for the synthesis of complex oligosaccharides.

4. Exploration of the potential of CTAG as a plant growth regulator.

5. Evaluation of the use of CTAG in the development of new enzymatic assays.

6. Study of the effect of CTAG on tumor development and progression.

7. Investigation of the use of CTAG in the production of new biofuels.

8. Development of new analytical methods for the detection of CTAG.

9. Study of the potential of CTAG in the development of new carbohydrate-based materials.

10. Improvements to the synthesis and purification of CTAG.

CAS Number61145-33-3
Product NameCyanomethyl 2,3,4,6-tetra-O-acetyl-1-thio-beta-D-galactopyranoside
IUPAC Name[3,4,5-triacetyloxy-6-(cyanomethylsulfanyl)oxan-2-yl]methyl acetate
Molecular FormulaC16H21NO9S
Molecular Weight403.41 g/mol
InChIInChI=1S/C16H21NO9S/c1-8(18)22-7-12-13(23-9(2)19)14(24-10(3)20)15(25-11(4)21)16(26-12)27-6-5-17/h12-16H,6-7H2,1-4H3
InChI KeyZNQCXCWNORCJGV-CWVYHPPDSA-N
SMILESCC(=O)OCC1C(C(C(C(O1)SCC#N)OC(=O)C)OC(=O)C)OC(=O)C
Synonyms[(2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl)thio]acetonitrile;
Canonical SMILESCC(=O)OCC1C(C(C(C(O1)SCC#N)OC(=O)C)OC(=O)C)OC(=O)C
Isomeric SMILESCC(=O)OC[C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)SCC#N)OC(=O)C)OC(=O)C)OC(=O)C


CAS No: 61145-33-3 MDL No: MFCD00057536 Chemical Formula: C16H21NO9S Molecular Weight: 403.41
References: 1. Lee Y-C, et al., Biochemistry 1976, 15, 18, p39562. Lee Y-C, et al., Biochemistry 1980, 19, p4899


INQUIRY

Scan the qr codeClose
the qr code