Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate(CAS: 59798-30-0)
![Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate](https://static.chemtradehub.com/structs/597/59798-30-0-3deb.webp)
CAS Number
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Other Suppliers for Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
Basic Information
Molecular Formula
C22H25N6NaO9S2
Molecular Weight
561.6 g/mol
Physical Properties
Water Solubility
Soluble in water or DMSO
Chemical Identifiers
SMILES
CC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)NC(=O)N4CCN(C4=O)S(=O)(=O)C)C(=O)[O-])C.[Na+]
InChIKey
SDQBKOKICLGDOA-ZBJAFUORSA-M
Database References
MDL Number
MFCD07793332
FAQ
Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 59798-30-0) is a crystalline compound with a molecular weight of approximately 968.46 g/mol. It has a high solubility in organic solvents such as dimethylformamide and is moderately soluble in water. The compound is known for its chemical stability but can react with strong acids and bases. It is used in various applications due to its unique reactivity and functional groups.
Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 59798-30-0) is synthesized through multi-step organic synthesis involving protection, functional group manipulation, and deprotection. Commonly, key steps include the formation of a key intermediate via coupling reactions and subsequent derivatization. The yield is typically around 70-80%, and the process is carried out under mild conditions to ensure high product purity.
Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 59798-30-0) is primarily used in the pharmaceutical industry due to its unique chemical structure and reactivity. It is also explored for its potential applications in polymer synthesis and as a precursor for various organic materials, including semiconductors and sensors.
When handling Sodium (2S,5R,6R)-3,3-dimethyl-6-({(2R)-2-[({[3-(methylsulfonyl)-2-oxo-1-imidazolidinyl]carbonyl}carbamoyl)amino]-2-phenylacetyl}amino)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate (CAS: 59798-30-0), it is important to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be carried out in a fume hood to minimize inhalation risks. Spills should be neutralized with a suitable base and cleaned up carefully. Always refer to the material safety data sheet (MSDS) or safety data sheet (SDS) for specific guidance and emergency procedures.
Safety Notice
Please verify product specifications and safety data before use. Contact the supplier for detailed safety information.
Always follow proper handling procedures
Contact Information
Contact Person
Li Yizhuo
362698781@qq.com
Mobile
15620955089
Telephone
022-88195255
Visit Website
http://www.biochem-mart.com/Address
Binheng District Rujing Street 319 Room





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