추천 제품
vapor pressure
2.6 mmHg ( 25 °C)
Quality Level
grade
purum
분석
≥97.0% (GC)
refractive index
n20/D 1.451 (lit.)
n20/D 1.451
bp
159 °C (lit.)
solubility
water: insoluble
density
1.506 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)CBr
InChI
1S/C4H7BrO2/c1-2-7-4(6)3-5/h2-3H2,1H3
InChI key
PQJJJMRNHATNKG-UHFFFAOYSA-N
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관련 카테고리
애플리케이션
Ethyl bromoacetate was used in the synthesis of:
- artificial diethylstilbestrol antigen
- 3-phenyl-1-naphthol, a key intermediate in the synthesis of vanol
- novel pyrazolothiazol-4(5H)-ones
- steroidal thiazolidinone derivatives
주의사항
may discolor to brown on storage
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
116.6 °F - closed cup
Flash Point (°C)
47 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Chemistry, an Asian journal, 6(8), 2130-2146 (2011-05-21)
Vanol is a member of the vaulted biaryl family of ligands and it has been proven to be very effective in a number of asymmetric catalytic reactions. The previous synthesis of vanol, while effective, is limited by the cost of
European journal of medicinal chemistry, 44(9), 3746-3753 (2009-05-08)
New N-acetyl (5-8) and N-thiocarbamoyl (9-12) derivatives of 4,5-dihydropyrazole were synthesized starting from alpha,beta-unsaturated ketones under the effect of hydrazine hydrate and thiosemicarbazide, respectively. N-Thiocarbamoylpyrazole derivatives (9-12) were cyclized using either ethyl bromoacetate or phenacyl bromides to afford the novel
Occupational allergic contact dermatitis in a chemist from ethyl bromoacetate and bromoacetonitrile.
Contact dermatitis, 52(2), 115-116 (2005-02-24)
European journal of medicinal chemistry, 44(6), 2597-2600 (2009-02-13)
Steroidal thiazolidinone derivatives were prepared by the multi-step reactions of steroid. It is prepared from steroidal thiosemicarbazones with ethyl bromoacetate in dioxane. Steroidal thiosemicarbazones were prepared by the reaction of thiosemicarbazide with steroidal ketones. The structures of these compounds were
Chemical communications (Cambridge, England), (6)(6), 622-623 (2002-07-18)
Copper(I) oxide can effectively co-catalyze the Suzuki type cross-coupling reactions of arylboronic acids with ethyl bromoacetate. As an alternative protocol for introducing the methylenecarboxy group into functionalized molecules, this reaction occurs in the absence of highly toxic thallium compounds or
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