Fmoc-3-amino-4-methylbenzoic Acid

≥95%

Reagent Code: #65041
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CAS Number 1072901-59-7

science Other reagents with same CAS 1072901-59-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.40 g/mol
Formula C₂₃H₁₉NO₄
badge Registry Numbers
MDL Number MFCD01861379
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Fmoc-3-amino-4-methylbenzoic acid is primarily used in peptide synthesis as a building block. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protecting group for the amino functionality during the synthesis process, ensuring that the amino group remains intact while other reactions take place. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides. Its structure allows for the introduction of specific aromatic and methyl-substituted moieties into peptide chains, which can be crucial for designing peptides with particular biological activities or structural properties. Additionally, it is employed in the development of peptidomimetics and small molecule drugs, where its unique chemical properties can enhance binding affinity or modulate pharmacokinetics.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿5,400.00

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Fmoc-3-amino-4-methylbenzoic Acid
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Fmoc-3-amino-4-methylbenzoic acid is primarily used in peptide synthesis as a building block. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protecting group for the amino functionality during the synthesis process, ensuring that the amino group remains intact while other reactions take place. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides. Its structure allows for the introduction of specific aromatic and methy

Fmoc-3-amino-4-methylbenzoic acid is primarily used in peptide synthesis as a building block. The Fmoc (fluorenylmethyloxycarbonyl) group serves as a protecting group for the amino functionality during the synthesis process, ensuring that the amino group remains intact while other reactions take place. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it helps in the stepwise assembly of peptides. Its structure allows for the introduction of specific aromatic and methyl-substituted moieties into peptide chains, which can be crucial for designing peptides with particular biological activities or structural properties. Additionally, it is employed in the development of peptidomimetics and small molecule drugs, where its unique chemical properties can enhance binding affinity or modulate pharmacokinetics.

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