627-18-9
627-18-9
Chemical Structure
3-Bromopropan-1-ol
- CAS No.: 627-18-9
- Formula:C3H7BrO
- Molecular Weight:138.99
IUPAC Name: 3-bromopropan-1-ol
InChIKey: RQFUZUMFPRMVDX-UHFFFAOYSA-N
SMILES: OCCCBr
Biological Activity: 3-Bromopropan-1-ol is an endogenous metabolite. 3-Bromopropan-1-ol is significantly up-regulated during the estrous period of buffaloes. 3-Bromopropan-1-ol acts as an alkylating agent. 3-Bromopropan-1-ol participates in the enantioselective synthesis of nornicotine enantiomers. 3-Bromopropan-1-ol can be used in studies related to estrus detection in buffaloes[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-Bromopropan-1-ol | 98.51% | 3-Bromopropan-1-ol is an endogenous metabolite. 3-Bromopropan-1-ol is significantly up-regulated during the estrous period of buffaloes. 3-Bromopropan-1-ol acts as an alkylating agent. 3-Bromopropan-1-ol participates in the enantioselective synthesis of nornicotine enantiomers. 3-Bromopropan-1-ol can be used in studies related to estrus detection in buffaloes. | ||||||||||||||||||||
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3-Bromopropan-1-ol-d6 | 98.5% | 3-Bromopropan-1-ol-d6 is the deuterium labeled 3-Bromopropan-1-ol (HY-W007337). 3-Bromopropan-1-ol is an endogenous metabolite. 3-Bromopropan-1-ol is significantly upregulated during the estrus period in buffaloes. 3-Bromopropan-1-ol can be used in buffalo estrus research. | ||||||||||||||||||||
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References
- [1]. Chojnacki K, et al. Synthesis of Novel Acyl Derivatives of 3-(4,5,6,7-Tetrabromo-1H-benzimidazol-1-yl)propan-1-ols-Intracellular TBBi-Based CK2 Inhibitors with Proapoptotic Properties. Int J Mol Sci. 2021 Jun 10;22(12):6261. [Content Brief]
- [2]. Swango JH, et al. A novel enantioselective synthesis of (S)-(-)- and (R)-(+)-nornicotine via alkylation of a chiral 2-hydroxy-3-pinanone ketimine template. Chirality. 1999;11(4):316-318. [Content Brief]
- [3]. Doshi P, et al. Untargeted metabolomics of buffalo urine reveals hydracyrlic acid, 3-bromo-1-propanol and benzyl serine as potential estrus biomarkers. J Proteomics. 2024;296:105124. [Content Brief]
