推荐产品
mp
84-88 °C (lit.)
品質等級
SMILES 字串
Brc1cc(Br)cc(C=O)c1
InChI
1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChI 密鑰
ZLDMZIXUGCGKMB-UHFFFAOYSA-N
應用
Reactant involved in:
- Suzuki-Miyaura cross-coupling reactions
- Synthesis of blue fluorescent dye derivatives for organic light emitting diodes
- Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts
- Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents
- Allylic alkylation
- Synthesis of C2-symmetric biphosphine ligand I
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Jakub Saadi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(12), 3842-3845 (2013-02-21)
Double-action haloketones: A super silyl group enabled the first highly diastereoselective Mukaiyama aldol reactions of α-chloro- and α-fluoroketones with a wide range of aldehydes, providing anti-β-siloxy-α-haloketones. This process is compatible with one-pot double-aldol methodology and allows for rapid access to
Synthesis, crystal structures, and antibacterial activity of a series of hydrazone compounds derived from 4-methylbenzohydrazide.
Lei Y, et al.
Journal of the Chilean Chemical Society, 60(2), 2961-2965 (2015)
Punit P Seth et al.
Bioorganic & medicinal chemistry letters, 14(22), 5569-5572 (2004-10-16)
The preparation and evaluation of novel aryl urea analogs as broad-spectrum antibacterial agents is described. Numerous compounds showed low micromolar minimum inhibitory concentrations (MIC) against both Gram-positive and Gram-negative bacteria. Selected analogs also exhibited in vivo efficacy in a lethal
Synthesis and luminescence characteristics of conjugated dendrimers with 2, 4, 6-triaryl-1, 3, 5-triazine periphery.
Kim CK, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(1), 254-263 (2006)
Conformational Behavior of Conjugated Polymers With Oligo (phenylene vinylene) Side Chains.
Peeter H and Koeckelberghs G.
Macromolecular Chemistry and Physics, 214(5), 538-546 (2013)
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