(S)-3-Amino-2,2-dimethyl-4-oxoazetidin-1-yl hydrogen sulfate

98%

Reagent Code: #236236
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CAS Number 102507-49-3

science Other reagents with same CAS 102507-49-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.21 g/mol
Formula C₅H₁₀N₂O₅S
badge Registry Numbers
MDL Number MFCD21608593
inventory_2 Storage & Handling
Density 1.67±0.1 g/cm3(Predicted)
Storage 2-8°C, preserved from light, dry sealed

description Product Description

Used as a key intermediate in the synthesis of beta-lactam antibiotics, particularly in the production of penem and carbapenem class antimicrobial agents. Its chiral structure enables stereoselective reactions critical for antibiotic efficacy. The sulfate group enhances solubility and facilitates further chemical modifications during drug manufacturing. Widely utilized in pharmaceutical research and development for creating potent, broad-spectrum antibiotics with activity against resistant bacterial strains.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,620.00
inventory 250mg
10-20 days ฿12,940.00
inventory 1g
10-20 days ฿34,900.00
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(S)-3-Amino-2,2-dimethyl-4-oxoazetidin-1-yl hydrogen sulfate
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Used as a key intermediate in the synthesis of beta-lactam antibiotics, particularly in the production of penem and carbapenem class antimicrobial agents. Its chiral structure enables stereoselective reactions critical for antibiotic efficacy. The sulfate group enhances solubility and facilitates further chemical modifications during drug manufacturing. Widely utilized in pharmaceutical research and development for creating potent, broad-spectrum antibiotics with activity against resistant bacterial stra

Used as a key intermediate in the synthesis of beta-lactam antibiotics, particularly in the production of penem and carbapenem class antimicrobial agents. Its chiral structure enables stereoselective reactions critical for antibiotic efficacy. The sulfate group enhances solubility and facilitates further chemical modifications during drug manufacturing. Widely utilized in pharmaceutical research and development for creating potent, broad-spectrum antibiotics with activity against resistant bacterial strains.

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