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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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N596328-100mg
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100mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$299.90
|
|
|
N596328-250mg
|
250mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$599.90
|
|
Propargyl PEG
| Synonyms | tert-butyl bis(2-(2-(prop-2-yn-1-yloxy)ethoxy)ethyl)carbamate | DTXSID801142162 | 4,7,13,16-Tetraoxa-10-azanonadeca-1,18-diynoic acid, 1,1-dimethylethyl ester | 2100306-86-1 | CS-0115586 | N-Boc-N-bis(PEG2-propargyl) | tert-butyl N,N-bis({2-[2-(prop-2-yn- |
|---|---|
| Specifications & Purity | ≥98% |
| Storage Temp | Store at -20°C,Argon charged |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
N-Boc-N-bis(PEG2-propargyl) is a branched PEG derivative with two terminal propargyl groups and a Boc protected amino group. The propargyl groups can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. The amino group is reactive with carboxylic acids, activated NHS esters, and carbonyls. The protected amine can be deprotected by acidic conditions. General description N-Boc-N-bis(PEG2-propargyl) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. N-Boc-N-bis(PEG2-propargyl) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Carbamic acids and derivatives |
| Direct Parent | Carbamate esters |
| Alternative Parents | Organic carbonic acids and derivatives Haloacetylenes and derivatives Dialkyl ethers Acetylides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carbamic acid ester - Carbonic acid derivative - Haloacetylene or derivatives - Acetylide - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as carbamate esters. These are compounds containing an ester of carbamic acid with the general structure R2NC(=O)OR' (R' not H). They are esters of carbamic acids. |
| External Descriptors | Not available |
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|
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| IUPAC Name | tert-butyl N,N-bis[2-(2-prop-2-ynoxyethoxy)ethyl]carbamate |
|---|---|
| INCHI | InChI=1S/C19H31NO6/c1-6-10-22-14-16-24-12-8-20(18(21)26-19(3,4)5)9-13-25-17-15-23-11-7-2/h1-2H,8-17H2,3-5H3 |
| InChIKey | NSGYNRBYZCGGOL-UHFFFAOYSA-N |
| Smiles | CC(C)(C)OC(=O)N(CCOCCOCC#C)CCOCCOCC#C |
| Isomeric SMILES | CC(C)(C)OC(=O)N(CCOCCOCC#C)CCOCCOCC#C |
| Alternate CAS | 2100306-86-1 |
| PubChem CID | 126961979 |
| Molecular Weight | 369.5 |
| Molecular Weight | 369.500 g/mol |
|---|---|
| XLogP3 | 0.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 16 |
| Exact Mass | 369.215 Da |
| Monoisotopic Mass | 369.215 Da |
| Topological Polar Surface Area | 66.500 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 0 |
| Complexity | 437.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
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