20769-85-1
20769-85-1
Chemical Structure
2-Bromoisobutyryl bromide
Synonym(s): Bromodimethylacetyl bromide; α-Bromoisobutyryl bromide
- CAS No.: 20769-85-1
- Formula:C4H6Br2O
- Molecular Weight:229.90
IUPAC Name: 2-bromo-2-methylpropanoyl bromide
InChIKey: YOCIJWAHRAJQFT-UHFFFAOYSA-N
SMILES: CC(C)(Br)C(Br)=O
Biological Activity: 2-Bromoisobutyryl bromide (Bromodimethylacetyl bromide) is an ATRP initiator. 2-Bromoisobutyryl bromide is used for surface-initiated polymerization. 2-Bromoisobutyryl bromide is used for the synthesis of iBBr monomer. 2-Bromoisobutyryl bromide is used for the bromoisobutyrylation of starch to prepare starch macroinitiators[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2-Bromoisobutyryl bromide | 98.0% | 2-Bromoisobutyryl bromide (Bromodimethylacetyl bromide) is an ATRP initiator. 2-Bromoisobutyryl bromide is used for surface-initiated polymerization. 2-Bromoisobutyryl bromide is used for the synthesis of iBBr monomer. 2-Bromoisobutyryl bromide is used for the bromoisobutyrylation of starch to prepare starch macroinitiators. | ||||||||||||||||||||
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1,1-Dibromoacetone | 1,1-Dibromoacetone is a dibromide product based on bromoacetone. | |||||||||||||||||||||
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1,1,1-Tribromoacetone | 1,1,1-Tribromoacetone is a tribromide product based on bromoacetone. | |||||||||||||||||||||
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2,2-Dibromopropanoic acid | 2,2-Dibromopropanoic acid is a dibromo product based on propionic acid. Propionic acid is a short chain fatty acid and acts as chemical intermediate. Propionic acid is also a mold inhibitor and widely used in food preservative. | |||||||||||||||||||||
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Dimethylmalonic acid (Standard) | ≥98% | Dimethylmalonic acid (Standard) (Dimethylpropanedioic acid (Standard)) is the analytical standard of Dimethylmalonic acid (HY-W007894). This product is intended for research and analytical applications. Dimethylmalonic acid (Dimethylpropanedioic acid) is a succinate dehydrogenase inhibitor. Dimethylmalonic acid competitively inhibits succinate dehydrogenase, reduces SDH-mediated succinate accumulation, blocks a key step in oxidative phosphorylation, and decreases anti-inflammatory cytokine secretion and ROS production. Dimethylmalonic acid can be used in research on autism spectrum disorders. | ||||||||||||||||||||
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2,2-Dimethylsuccinic acid | 98.0% | 2,2-Dimethylsuccinic acid belongs to the class of organic compounds known as methyl-branched fatty acids. | ||||||||||||||||||||
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Dimebutic acid | 99.85% | Dimebutic acid is an orally active short-chain fatty acid. Dimebutic acid stimulates fetal globin production and alters the balance of Bcl family proteins. Dimebutic acid prolongs red blood cell survival. Dimebutic acid exhibits toxicity in rats. Dimebutic acid can be used in the study of β-thalassemia and sickle cell disease. | ||||||||||||||||||||
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Valeryl Bromide | Valeryl Bromide is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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Pivalic acid | 99.93% | Pivalic acid (Trimethylmethanecarboxylic acid) is a carboxylic acid. Pivalic acid induces Carnitine deficiency. Pivalic acid conjugated with Antibiotics, such as Pivmecillinam (HY-B0810) and Pivampicillin (HY-119011), are used in urinary tract infection. Pivalic acid can be used in physical exercise research. | ||||||||||||||||||||
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Trimethylacetaldehyde | Trimethylacetaldehyde (Pivalic aldehyde; Pivalaldehyde) is an inhibitor of E. coli betaine aldehyde dehydrogenase (ALDH) with a Ki of 4.5 mM. Trimethylacetaldehyde serves as a substrate for Drosophila melanogaster alcohol dehydrogenase (AdhS), undergoing oxidation and disproportionation reactions with the release of NADH, and also forms an inactive binary enzyme-aldehyde complex via a compulsory ordered reaction mechanism. | |||||||||||||||||||||
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References
- [1]. Liu X, et al. Cationic brush hybrid nanoparticles scavenge cell-free DNA to enhance rheumatoid arthritis treatment. Acta biomaterialia. 2023 Oct 15;170:215-227.
- [2]. Chen Y, et al. Intracellular Generation of Alkyl Radicals Enabled by a Self-Catalytic ATRP Nanoinitiator. ACS macro letters. 2024 Oct 15;13(10):1233-1239.
- [3]. Lee SB, et al. Permanent, nonleaching antibacterial surfaces. 1. Synthesis by atom transfer radical polymerization. Biomacromolecules. 2004;5(3):877-82.
- [4]. Li W, et al. Investigation on the Synthesis Process of Bromoisobutyryl Esterified Starch and Its Sizing Properties: Viscosity Stability, Adhesion and Film Properties. Polymers. 2019 Nov 25;11(12):1936.
