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2,5-dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate

  CAS No.: 370856-45-4   Cat No.: BADC-00679 4.5  

2,5-dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate is a linker for antibody-drug-conjugation (ADC).

2,5-dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate

Structure of 370856-45-4

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ADC Linker
Molecular Formula
C28H27NO7
Molecular Weight
489.52
Shipping
Room temperature

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Canonical SMILES
COC1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=C(C=C3)OC)OCCC(=O)ON4C(=O)CCC4=O
InChI
InChI=1S/C28H27NO7/c1-33-23-12-8-21(9-13-23)28(20-6-4-3-5-7-20,22-10-14-24(34-2)15-11-22)35-19-18-27(32)36-29-25(30)16-17-26(29)31/h3-15H,16-19H2,1-2H3
InChIKey
BDBGKCXKPUCIFV-UHFFFAOYSA-N
Shipping
Room temperature

One of the primary applications of 2,5-Dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate is in the chemical research and synthesis of urea. This compound plays an essential role as an intermediate in the generation of urea, which itself is industrially synthesized in large quantities. Urea, being a critical component in fertilizers, underscores the significance of this compound in aiding agricultural productivity. Furthermore, its role extends to a variety of biosynthetic processes in the production of pharmaceuticals and fine chemicals.

Another significant application of this compound is in the manufacture of polyurethane plastics. Polyurethanes represent a broad category of polymers that incorporate carbamate groups into their structure. The diverse properties of polyurethanes make them highly valuable, as these materials can be formulated to range from flexible foams to rigid solids. They are extensively used in furniture, automotive, and construction industries. The versatile nature of 2,5-Dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate allows for the production of polyurethanes with specified characteristics required for different applications.

The compound also finds application in the development of carbamate-based insecticides. These insecticides are effective due to their mechanism of action, which involves inhibiting the enzyme acetylcholinesterase in pests. This interruption in nerve signal transmission results in the eradication of various insects that threaten crops. As sustainable agricultural practices demand efficient pest control measures, carbamate insecticides synthesized using this compound are instrumental in ensuring crop protection and productivity.

Moreover, 2,5-Dioxopyrrolidin-1-yl 3-(bis(4-methoxyphenyl)(phenyl)methoxy)propanoate is employed in the field of medicine as part of drugs designed to modulate acetylcholine activity in the nervous system. Rivastigmine and physostigmine, both acetylcholinesterase inhibitors used in treating conditions like Alzheimer’s disease and myasthenia gravis, can be related to the broader class of compounds involving carbamates. These medical applications highlight the role of this compound in addressing neurological conditions by enhancing neurotransmitter activity, thereby improving cognitive functions and muscle response. This functionality makes it a critical component in the development of therapeutic agents.

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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Historical Records: Me-Tet-PEG4-NHS | DBCO-NH-PEG4-amine | Propargyl-PEG7-acid | 2,5-dioxopyrrolidin-1-yl 4-((3-(dimethylcarbamoyl)pyridin-4-yl)disulfanyl)pentanoate | 3-azidopropanoate-N-hydroxysuccinimide ester | NHPI-PEG3-C2-PFP ester | 4-nitrophenyl 2-(pyridin-2-yldisulfanyl)propyl carbonate | Fmoc-Gly-Gly-Phe-OtBu | NHPI-PEG3-C2-NHS ester | 2,5-dioxopyrrolidin-1-yl 3-Iodo-4-methoxybenzoate | NHPI-PEG2-C2-NHS ester
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