1219795-54-6
Chemical Structure
2-Bromo-1,4-difluorobenzene-d3
- CAS 番号: 1219795-54-6
- Formula:C6D3BrF2
- Molecular Weight:196.01
IUPAC Name: 4-bromo-1,2-difluorobenzene-3,5,6-d3
InChIKey: XCRCSPKQEDMVBO-CBYSEHNBSA-N
SMILES: BrC1=C(C([2H])=C([2H])C(F)=C1[2H])F
Biological Activity: 2-Bromo-1,4-difluorobenzene-d3 is the d3-labeled 2-Bromo-1,4-difluorobenzene (HY-79541). 2-Bromo-1,4-difluorobenzene is a fluorine-substituted haloarene and serves as an inexpensive, large-volume organic synthesis raw material. 2-Bromo-1,4-difluorobenzene can be used to prepare 1,4-difluoroanthraquinone, which is a precursor of Ametantrone (HY-13550). 2-Bromo-1,4-difluorobenzene can be used as a biomaterial or organic compound in life science-related research[1][2].
| 製品番号 | 製品名 | 純度 | 製品説明 | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-Bromo-1,4-difluorobenzene-d3 | 2-Bromo-1,4-difluorobenzene-d3 is the d3-labeled 2-Bromo-1,4-difluorobenzene (HY-79541). 2-Bromo-1,4-difluorobenzene is a fluorine-substituted haloarene and serves as an inexpensive, large-volume organic synthesis raw material. 2-Bromo-1,4-difluorobenzene can be used to prepare 1,4-difluoroanthraquinone, which is a precursor of Ametantrone (HY-13550). 2-Bromo-1,4-difluorobenzene can be used as a biomaterial or organic compound in life science-related research. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Bromo-1,4-difluorobenzene | 99.97% | 2-Bromo-1,4-difluorobenzene is a fluorine-substituted haloarene and serves as an inexpensive, large-volume organic synthesis raw material. 2-Bromo-1,4-difluorobenzene can be used to prepare 1,4-difluoroanthraquinone, which is a precursor of Ametantrone (HY-13550). 2-Bromo-1,4-difluorobenzene can be used as a biomaterial or organic compound in life science-related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Subash P. Khanapure, et al., Synthesis of fluorine-substituted anthraquinones and aza-anthraquinones, Journal of Fluorine Chemistry, Volume 68, Issue 2, 1994, Pages 131-134, ISSN 0022-1139.
- [2]. Le DN, et al. Enantio- and Diastereoselective Total Synthesis of Belzutifan Enabled by Rh-Catalyzed Hydrogenation. Organic letters. 2024 May 17;26(19):4059-4064.
