Methyl benzyloxycarbamate

95%

Reagent Code: #84677
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CAS Number 5555-71-5

science Other reagents with same CAS 5555-71-5

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Weight 181.19 g/mol
Formula C₉H₁₁NO₃
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MDL Number MFCD26794518
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Used primarily in organic synthesis as a protective group for amines. It helps in selectively masking amino groups during complex chemical reactions, ensuring that only desired functional groups react. This chemical is particularly useful in peptide synthesis, where it safeguards amino acids from unwanted side reactions. It also finds application in the preparation of pharmaceuticals, enabling the development of specific drug molecules by protecting reactive amine sites. Additionally, it is employed in research laboratories for studying reaction mechanisms and developing new synthetic pathways. Its stability under various conditions makes it a reliable choice for chemists working on intricate molecular constructions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,850.00
inventory 250mg
10-20 days ฿10,530.00
inventory 1g
10-20 days ฿21,060.00

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Methyl benzyloxycarbamate
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Used primarily in organic synthesis as a protective group for amines. It helps in selectively masking amino groups during complex chemical reactions, ensuring that only desired functional groups react. This chemical is particularly useful in peptide synthesis, where it safeguards amino acids from unwanted side reactions. It also finds application in the preparation of pharmaceuticals, enabling the development of specific drug molecules by protecting reactive amine sites. Additionally, it is employed in r

Used primarily in organic synthesis as a protective group for amines. It helps in selectively masking amino groups during complex chemical reactions, ensuring that only desired functional groups react. This chemical is particularly useful in peptide synthesis, where it safeguards amino acids from unwanted side reactions. It also finds application in the preparation of pharmaceuticals, enabling the development of specific drug molecules by protecting reactive amine sites. Additionally, it is employed in research laboratories for studying reaction mechanisms and developing new synthetic pathways. Its stability under various conditions makes it a reliable choice for chemists working on intricate molecular constructions.

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