98827-08-8

Basic information

• Product Name: 7-(1-hydroxy-2-methylthioethyl)-2,2-dimethyl-3-oxa-7-phenylthio-1-azabicyclo<4.2.0>octan-8-one
• CAS NO: 98827-08-8
• Molecular Weight: 353.507
• Mol File: 98827-08-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 7-(1-hydroxy-2-methylthioethyl)-2,2-dimethyl-3-oxa-7-phenylthio-1-azabicyclo<4.2.0>octan-8-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-(1-hydroxy-2-methylthioethyl)-2,2-dimethyl-3-oxa-7-phenylthio-1-azabicyclo<4.2.0>octan-8-one(98827-08-8)
• EPA Substance Registry System: 7-(1-hydroxy-2-methylthioethyl)-2,2-dimethyl-3-oxa-7-phenylthio-1-azabicyclo<4.2.0>octan-8-one(98827-08-8)

Safety Data

• Hazardous Substances Data: 98827-08-8(Hazardous Substances Data)

Upstream product

• 23328-62-3 2-(methylthio)acetaldehyde 
• 882-33-7 diphenyldisulfane 
• 64066-65-5 2,2-dimethyl-3-oxa-1-aza-bicyclo[4.2.0]octan-8-one 

Downstream Products

• 98811-29-1 p-nitrobenzyl (5RS,6RS)-2-acetamodoethylthio-6-<1-hydroxy-2-methylsulfonylethyl>-2-carbapenem-3-carboxylate 
• 98810-83-4 (3RS,4RS)-3-<1-(2-methoxyethoxymethoxy)-2-methylsulfonylethyl>-4-(p-nitrobenzyloxycarbonyl-2-oxopropyl)azetidin-2-one 

Relevant articles and documents

Carbapenems, their production and use

A compound of the general formula: STR1 wherein X is a lower alkylene group which may optionally be substituted by a hydroxyl group, or a lower alkenylene group, Y is (1) a lower alkyl group, (2) a cycloalkyl group containing 3 to 8 carbon atoms, (3) a lower alkenyl group, (4) an aryl group, (5) an aralkyl group or (6) a 3- to 8-membered heterocyclic group, or the partial structural formula Y--SO2 --X--, with X and Y being combined with each other, represents a group of the formula: STR2 wherein l is an integer of 0 to 3, and m and n each is an integer of 0 to 6, provided that the sum of m and n is in the range of 2 to 6, and R is a hydrocarbon group which may optionally be substituted or a 3- to 8-membered heterocyclic group, or a pharmaceutically acceptable salt thereof a method of production thereof and use thereof. The compound (I) has antimicrobial and β-lactamase inhibitory activities.