(5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-({2-[(iminomethyl)amino]ethyl}sulfanyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate (1:1)(CAS: 74431-23-5)
![(5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-({2-[(iminomethyl)amino]ethyl}sulfanyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate (1:1) (5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-({2-[(iminomethyl)amino]ethyl}sulfanyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate (1:1)](https://static.chemtradehub.com/structs/744/74431-23-5-4eb7.webp)
CAS Number
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Other Suppliers for (5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-({2-[(iminomethyl)amino]ethyl}sulfanyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate (1:1)
Basic Information
Molecular Formula
C12H19N3O5S
Molecular Weight
317.37 g/mol
Physical State
White to Yellow Solid
Physical Properties
Melting Point
194-200°C
Boiling Point
567 °C
Flash Point
>110°(230°F)
Water Solubility
Soluble in water at 5mg/ml
Chemical Identifiers
SMILES
CC(C1C2CC(=C(N2C1=O)C(=O)O)SCCN=CN)O.O
InChIKey
GSOSVVULSKVSLQ-JJVRHELESA-N
Database References
MDL Number
MFCD09753321
FAQ
This compound is a hydrate with a molecular weight of approximately 434.47 g/mol. It crystallizes in a specific form with a high melting point and good solubility in organic solvents. The compound is known for its reactivity towards nucleophiles and its stability under neutral and basic conditions. It is often used in analytical chemistry due to its unique functional groups.
This compound is synthesized through a multi-step reaction involving condensation and cyclization reactions. Commonly, it is prepared from acyclic precursors using amines and amidation reactions. The synthesis typically involves the use of mild bases and catalysts to achieve high selectivity and yield. Detailed procedures can be found in various organic synthesis literature.
This compound is primarily used in the pharmaceutical industry for its potential as a drug candidate due to its unique chemical structure. It also finds applications in sensor technology and semiconductor materials, where its functional groups can be utilized for specific binding interactions and electronic properties.
Proper handling of this compound should be conducted in a well-ventilated area, preferably under a fume hood. Personal protective equipment (PPE) such as gloves, goggles, and a lab coat should be worn to avoid direct contact and inhalation. Spills should be managed carefully using appropriate absorbent materials and the Material Safety Data Sheet (MSDS) should be consulted for specific cleanup procedures. Storage should be in a cool, dry place away from direct sunlight and heat sources.
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
mfg@handepharm.com










![(5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-({2-[(iminomethyl)amino]ethyl}sulfanyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid hydrate (1:1) — ShangHaiJiZhiShengHua Technology Co Ltd](https://static.chemtradehub.com/suppliers/67cecbee2b2de6e8e95a5b72/67cecbee2b2de6e8e95a5b72-logo.webp)