324728
6-溴己酸乙酯
99%
别名:
6-Bromohexanoic acid ethyl ester, Ethyl 6-bromocapronate
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关于此项目
线性分子式:
Br(CH2)5COOCH2CH3
化学文摘社编号:
分子量:
223.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
247-085-2
Beilstein/REAXYS Number:
1756051
MDL number:
Assay:
99%
Form:
liquid
产品名称
6-溴己酸乙酯, 99%
InChI key
DXBULVYHTICWKT-UHFFFAOYSA-N
InChI
1S/C8H15BrO2/c1-2-11-8(10)6-4-3-5-7-9/h2-7H2,1H3
SMILES string
CCOC(=O)CCCCCBr
assay
99%
form
liquid
refractive index
n20/D 1.458 (lit.)
bp
128-130 °C/16 mmHg (lit.)
density
1.254 g/mL at 25 °C (lit.)
functional group
bromo
ester
Quality Level
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Application
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。
General description
6-溴己酸乙酯是一种 ω-溴酸酯。
Other Notes
储存时颜色可能变深
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
136.9 °F - closed cup
flash_point_c
58.3 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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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