93603-76-0

Basic information

• Product Name: (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
• Synonyms: (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
• CAS NO: 93603-76-0
• Molecular Weight: 443.704
• Mol File: 93603-76-0.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate(93603-76-0)
• EPA Substance Registry System: (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate(93603-76-0)

Safety Data

• Hazardous Substances Data: 93603-76-0(Hazardous Substances Data)

Usage

Description

(5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate is a complex carboxylic acid ester derived from a rearranged penicillin molecule. It features a bicyclic structure with a thiol and a carbonyl group, and it has a chiral configuration. (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate also contains an allyl group, a silyloxy moiety, and a propylthio group attached to its central core. (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate is utilized in organic synthesis and pharmaceutical research as a key building block for designing new molecules with potential biological activities.

Uses

Used in Pharmaceutical Research:
(5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate is used as a building block for the development of new pharmaceutical compounds. Its unique structure and functional groups make it a valuable asset in creating molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate serves as an important intermediate for the synthesis of various complex organic molecules. Its versatile structure allows for further functionalization and modification, leading to the creation of a wide range of compounds with diverse properties and applications.
Used in Chemical Research:
(5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate is also employed in chemical research to study the properties and reactivity of complex organic molecules. Its unique structure and chiral configuration provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Used in Material Science:
In the field of material science, (5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate may be used as a component in the development of novel materials with specific properties. Its structural features could potentially be exploited to create materials with enhanced performance characteristics, such as improved stability, reactivity, or selectivity.
Used in Analytical Chemistry:
(5R,6S)-allyl 6-((R)-1-(tert-butyldimethylsilyloxy)ethyl)-7-oxo-3-(propylthio)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate can be utilized in analytical chemistry as a reference compound or a standard for the development and validation of new analytical methods. Its complex structure and chiral configuration make it an interesting candidate for studying the separation and detection of enantiomers and other stereoisomers.

Downstream Products

• 120788-07-0 (3S)-3-({(5R, 6S)-2-carboxy-6-[(1R)-1-hydroxyethyl]-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-en-3-yl}sulfanyl)tetrahydrothiophenium-1-olate