phenyl hydroxycarbamate

95%

Reagent Code: #226512
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CAS Number 38064-07-2

science Other reagents with same CAS 38064-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₇H₇NO₃
badge Registry Numbers
MDL Number MFCD18968936
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Acts as a protecting group reagent for amines due to its ability to form stable derivatives under mild conditions. Employed in the development of enzyme inhibitors, particularly in research targeting histone deacetylases (HDACs), which are important in cancer therapy. Also utilized in the preparation of carbamate-based prodrugs to improve bioavailability and controlled release. Its phenyl and hydroxy functionalities allow for easy modification and conjugation in drug design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿10,800.00
25g
10-20 days ฿42,750.00
100g
10-20 days ฿130,500.00
phenyl hydroxycarbamate
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Acts as a protecting group reagent for amines due to its ability to form stable derivatives under mild conditions. Employed in the development of enzyme inhibitors, particularly in research targeting histone deacetylases (HDACs), which are important in cancer therapy. Also utilized in the preparation of carbamate-based prodrugs to improve bioavailability and controlled release. Its phenyl and hydroxy functionalities allow

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Acts as a protecting group reagent for amines due to its ability to form stable derivatives under mild conditions. Employed in the development of enzyme inhibitors, particularly in research targeting histone deacetylases (HDACs), which are important in cancer therapy. Also utilized in the preparation of carbamate-based prodrugs to improve bioavailability and controlled release. Its phenyl and hydroxy functionalities allow for easy modification and conjugation in drug design.

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