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About This Item
线性分子式:
Br(CH2)5COOCH2CH3
CAS号:
分子量:
223.11
Beilstein:
1756051
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗
99%
形狀
liquid
折射率
n20/D 1.458 (lit.)
bp
128-130 °C/16 mmHg (lit.)
密度
1.254 g/mL at 25 °C (lit.)
官能基
bromo
ester
SMILES 字串
CCOC(=O)CCCCCBr
InChI
1S/C8H15BrO2/c1-2-11-8(10)6-4-3-5-7-9/h2-7H2,1H3
InChI 密鑰
DXBULVYHTICWKT-UHFFFAOYSA-N
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一般說明
6-溴己酸乙酯是一种 ω-溴酸酯。
應用
在肉碱转运蛋白研究中，6-溴己酸乙酯可用于制备各种肉碱衍生物。它也用于戊烷-2,4-二酮的烷基化。
其他說明
储存时颜色可能变深
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
136.9 °F - closed cup
閃點（°C）
58.3 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
An Improved Procedure for Mono C-Alkylation of Pentane-2.4-Dione with ?-Bromoacid Esters.
Shrout DP and Lightner DA.
Synthetic Communications, 20(13), 2075-2080 (1990)
Angelo Lanzilotto et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 23(1), 109-122 (2017-12-09)
A new water-soluble photocatalyst for singlet oxygen generation is presented. Its absorption extends to the red part of the spectrum, showing activity up to irradiation at 660 nm. Its efficiency has been compared to that of a commercial analogue (Rose Bengal)
Atsushi Enomoto et al.
The Journal of biological chemistry, 277(39), 36262-36271 (2002-06-29)
l-Carnitine is an essential component of mitochondrial fatty acid beta-oxidation and plays a pivotal role in the maturation of spermatozoa within the male reproductive tract. Epididymal plasma contains the highest levels of l-carnitine found in the human body, and initiation
D Timothy Anstine et al.
Monatshefte fur chemie, 145(7), 1117-1135 (2014-08-12)
Three new linear pentapyrrole rubinoid analogs: 2,3,7,8,17,18,22,23-octamethyl-12,13-bis-(2-carboxyethyl)-1,10,15,24,25,27,28,29-octahydro-27H-pentapyrrin-1,24-dione and 2,3,8,12,13,17,22,23-octamethyl-7,18-bis-(2-carboxyethyl)-1,10,15,24,25,26,27,28,29-octahydro-27H-pentapyrrin-1,24-dione, and its 7,18-dihexanoic acid analog were synthesized, respectively, from 2,3,7,8-tetramethyl-(10H)-dipyrrin-2-one, from 2,3,8-trimethyl-7-[2-(methoxycarbonyl)ethyl]-(10H)-dipyrrinone, and 2,3,8-trimethyl-7-[5-(methoxycarbonyl)pentyl]-(10H)-dipyrrinone. 13C NMR and 1H NMR measurements in (CD3)2SO confirmed the pentapyrrole structures, while 1H NMR data indicate
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