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蒸汽壓力
2.6 mmHg ( 25 °C)
品質等級
等級
purum
化驗
≥97.0% (GC)
折射率
n20/D 1.451 (lit.)
n20/D 1.451
bp
159 °C (lit.)
溶解度
water: insoluble
密度
1.506 g/mL at 25 °C (lit.)
SMILES 字串
CCOC(=O)CBr
InChI
1S/C4H7BrO2/c1-2-7-4(6)3-5/h2-3H2,1H3
InChI 密鑰
PQJJJMRNHATNKG-UHFFFAOYSA-N
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應用
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
注意
储存期间可变为棕色
訊號詞
Danger
危險分類
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Flam. Liq. 3
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
116.6 °F - closed cup
閃點(°C)
47 °C - closed cup
個人防護裝備
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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