추천 제품
vapor pressure
3.8 mmHg ( 25 °C)
Quality Level
분석
≥98%
양식
liquid
refractive index
n20/D 1.547 (lit.)
bp
147-150 °C (lit.)
density
2.317 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
BrCC(Br)=O
InChI
1S/C2H2Br2O/c3-1-2(4)5/h1H2
InChI key
LSTRKXWIZZZYAS-UHFFFAOYSA-N
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관련 카테고리
일반 설명
Bromoacetyl bromide is employed as an acylating reagent and in the production of heterocyclic compounds.
애플리케이션
Bromoacetyl bromide can be used to convert:
It can also be used as a reagent to synthesize imidazolium or piridinium based ionic liquids.
- Amines to azido acetamides.
- p-Arsanilic acid to 4-(2-bromoacetylamino)benzenearsonic acid, a precursor to 4-(N-(S-penicillaminylacetyl)amino)phenylarsonous acid (PENAO), a metal-based drug.
- 3,5-Dimethylphenol to 3,5-dimethylphenyl 2-bromoacetate.
- Cystamine dihydrochloride to N,N′-bis(bromoacetyl) cystamine, a bifunctional quaternizing agent.
It can also be used as a reagent to synthesize imidazolium or piridinium based ionic liquids.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
보충제 위험성
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
221.0 °F - closed cup
Flash Point (°C)
105 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Aggregation behavior and antimicrobial activity of ester-functionalized imidazolium-and pyridinium-based ionic liquids in aqueous solution.
Garcia MT, et al.
Langmuir, 29(8), 2536-2545 (2013)
pH and reduction dual-responsive nanogel cross-linked by quaternization reaction for enhanced cellular internalization and intracellular drug delivery.
Li M, et al.
Polym. Chem., 4(4), 1199-1207 (2013)
Direct Polymerization of the Arsenic Drug PENAO to Obtain Nanoparticles with High Thiol-Reactivity and Anti-Cancer Efficiency.
Noy JM, et al.
Bioconjugate Chemistry, 29(2), 546-558 (2018)
Regio-and Stereoselective Nickel-Catalyzed Coupling of Boronic Acids with Allenoates.
Liu Y, et al.
Synthesis, 29(2), 546-558 (2018)
Site-Selective Conversion of Azido Groups at Carbonyl ?-Positions to Diazo Groups in Diazido and Triazido Compounds.
Yokoi T, et al.
The Journal of Organic Chemistry, 83(19), 12103-12121 (2018)
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