≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
The hydrolytic dehalogenation of 2-bromopropionamide was catalyzed by dl-2-haloacid dehalogenase fromPseudomonas putidaPP3 (dl-DEX 312).
| Pubchem Sid | 488187234 |
|---|---|
| Sorrisi canonici | CC(C(=O)N)Br |
| IUPAC Name | 2-bromopropanamide |
| InChIKey | AUHYZQCEIVEMFH-UHFFFAOYSA-N |
| INCHI | 1S/C3H6BrNO/c1-2(4)3(5)6/h2H,1H3,(H2,5,6) |
| Isomeri SMILES | CC(C(=O)N)Br |
| WGK Germania | 3 |
| RTECS | UE3168680 |
| Peso molecolare | 151.99 |
| Reaxy-Rn | 1720244 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1720244&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Classe | Carboxylic acids and derivatives |
| Subclass | Carboxylic acid derivatives |
| Intermediate Tree Nodes | Carboxylic acid amides |
| Direct Parent | Primary carboxylic acid amides |
| Alternative Parents | Organopnictogen compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl bromides |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Primary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 C2514672 | Certificate of Analysis | Jun 27, 2024 | B474352 |
| D2321760 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321797 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321798 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321799 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321805 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321808 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321809 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| D2321810 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| J2509131 | Certificate of Analysis | Mar 22, 2023 | B474352 |
| Punto di fusione (°C) | 123-125 °C |
|---|---|
| Peso molecolare | 151.990 g/mol |
| XLogP3 | 0.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 150.963 Da |
| Monoisotopic Mass | 150.963 Da |
| Topological Polar Surface Area | 43.100 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 63.800 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
