BOC-GLY-OME

97%

  • Product Code: 104859
  Alias:    BOC-Glycine Methyl N-tert-Butoxycarbonyl Glycine Methyl N-BOC-Glycine Methyl N-BOC-Glycine Methyl N-BOC-Glycine Methyl N-BOC-Glycine Methyl N-(tert-Butoxy Carbonyl) glycine methyl ester BOC-GLY-OME BOC-glycine methyl ester
  CAS:    31954-27-5
Molecular Weight: 189.21 g./mol Molecular Formula: C₈H₁₅NO₄
EC Number: MDL Number: MFCD00038267
Melting Point: Boiling Point: 190 °C
Density: 1.28 g/mL at 25 °C Storage Condition: 2~8 ℃
Product Description: BOC-GLY-OME is widely used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring that reactions occur at the desired sites without interference. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise construction of peptides. Additionally, it is employed in the preparation of glycine derivatives, which are essential intermediates in the production of various pharmaceuticals and bioactive peptides. Its stability under reaction conditions and ease of removal make it a preferred choice in organic and medicinal chemistry research.
Product Specification:
Test Specification
Purity (%) 97-100
Appearance Colorless To Yellow Liquid
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿300.00
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25.000 10-20 days ฿850.00
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100.000 10-20 days ฿2,980.00
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-
500.000 10-20 days ฿12,800.00
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BOC-GLY-OME
BOC-GLY-OME is widely used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amino group during the formation of peptide bonds, ensuring that reactions occur at the desired sites without interference. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise construction of peptides. Additionally, it is employed in the preparation of glycine derivatives, which are essential intermediates in the production of various pharmaceuticals and bioactive peptides. Its stability under reaction conditions and ease of removal make it a preferred choice in organic and medicinal chemistry research.
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