N-(Chloroacetyl)glycine ethyl ester

98%

Reagent Code: #218888
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CAS Number 41602-50-0

science Other reagents with same CAS 41602-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.60 g/mol
Formula C₆H₁₀ClNO₃
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MDL Number MFCD00216646
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-lactam antibiotics. It serves as a building block for introducing the glycine moiety in penicillin and cephalosporin analogs. Also employed in the preparation of peptide-like structures and heterocyclic compounds due to its reactive chloroacetyl group, which allows for further nucleophilic substitution reactions. Its ester functionality facilitates solubility and reactivity in organic solvents, making it suitable for multi-step synthetic routes in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,670.00
inventory 25g
10-20 days ฿14,140.00
N-(Chloroacetyl)glycine ethyl ester
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-lactam antibiotics. It serves as a building block for introducing the glycine moiety in penicillin and cephalosporin analogs. Also employed in the preparation of peptide-like structures and heterocyclic compounds due to its reactive chloroacetyl group, which allows for further nucleophilic substitution reactions. Its ester functionality facilitates solubility and reactivity in organic solvents, making it s

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-lactam antibiotics. It serves as a building block for introducing the glycine moiety in penicillin and cephalosporin analogs. Also employed in the preparation of peptide-like structures and heterocyclic compounds due to its reactive chloroacetyl group, which allows for further nucleophilic substitution reactions. Its ester functionality facilitates solubility and reactivity in organic solvents, making it suitable for multi-step synthetic routes in medicinal chemistry.

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