Gly-NH-CH2-Boc - CAS 14664-05-2

Gly-NH-CH2-Boc - CAS 14664-05-2 Catalog number: BADC-01627

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Gly-NH-CH2-Boc is a cleavable ADC linker that can be used in antibody-conjugated active molecules (ADC).

Category
ADCs Linker
Product Name
Gly-NH-CH2-Boc
CAS
14664-05-2
Catalog Number
BADC-01627
Molecular Formula
C8H16N2O3
Molecular Weight
188.22

Ordering Information

Catalog Number Size Price Quantity
BADC-01627 -- $-- Inquiry
Description
Gly-NH-CH2-Boc is a cleavable ADC linker that can be used in antibody-conjugated active molecules (ADC).
Synonyms
tert-butyl glycylglycinate; Gly-Gly-O-tBu
IUPAC Name
tert-butyl 2-[(2-aminoacetyl)amino]acetate
Canonical SMILES
CC(C)(C)OC(=O)CNC(=O)CN
InChI
InChI=1S/C8H16N2O3/c1-8(2,3)13-7(12)5-10-6(11)4-9/h4-5,9H2,1-3H3,(H,10,11)
InChIKey
VJEYRLMJNBJAHS-UHFFFAOYSA-N
Density
1.083±0.06 g/cm3
Melting Point
114-116°C
Appearance
Colorless to light yellow Oil
Boiling Point
315.5±22.0 °C at 760 mmHg

Gly-NH-CH2-Boc, also recognized as N-Boc-glycine methyl ester, stands as a versatile compound with wide-ranging applications in organic synthesis and biotechnological endeavors.

Peptide Synthesis: A staple in peptide synthesis, Gly-NH-CH2-Boc emerges as a frequently employed protected glycine derivative. The Boc (tert-butoxycarbonyl) group acts as a shield for the amino group during peptide chain elongation, averting undesired side reactions. This enables the precise and selective assembly of peptides with custom sequences and functionalities, exemplifying the finesse of organic synthesis.

Pharmaceutical Development: Pioneering drug discovery, Gly-NH-CH2-Boc plays a pivotal role as a fundamental building block for crafting biologically active molecules and pharmaceutical intermediates. Through the integration of this safeguarded amino acid into drug candidates, researchers delve into the intricate structure-activity relationships crucial for designing and enhancing novel therapeutic agents.

Bioconjugation: Embracing bioconjugation strategies, Gly-NH-CH2-Boc proves instrumental in attaching functional molecules to biomolecules like proteins or antibodies. The Boc group, known for its ease of removal under mild conditions, liberates the amino group for subsequent chemical alterations.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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