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Merck
CN

393304

7-溴庚酸乙酯

97%

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线性分子式:
Br(CH2)6CO2C2H5
化学文摘社编号:
分子量:
237.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
249-883-6
MDL number:
Assay:
97%
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产品名称

7-溴庚酸乙酯, 97%

InChI key

OOBFNDGMAGSNKA-UHFFFAOYSA-N

InChI

1S/C9H17BrO2/c1-2-12-9(11)7-5-3-4-6-8-10/h2-8H2,1H3

SMILES string

CCOC(=O)CCCCCCBr

assay

97%

refractive index

n20/D 1.459 (lit.)

bp

112 °C/5 mmHg (lit.)

mp

29 °C (lit.)

density

1.217 g/mL at 25 °C (lit.)

functional group

bromo
ester

Quality Level

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Application

Ethyl 7-bromoheptanoate may be used in the following studies:
  • As a starting material in the synthesis of benzyl 7-iodoheptanoate.
  • As one of the reactant in the synthesis of diethyl 7,7′-(2,5-diiodo-1,4-phenylene)bis(oxy)diheptanoate.
  • As one of the reagent in the synthesis of CarnDOD-7C, a carnitine-derived nitrone.
  • As an alkylating agent in the alkylation of ethyl 3-oxoglutarate to form 2-(6-ethoxycarbonylhexyl)-3-oxoglutarate.
  • Synthesis of 1-substituted cyclopentadiene by alkylating lithium cyclopentadienide.5

General description

Ethyl 7-bromoheptanoate is a bromoester. It is used as an alkylating agent for organic compounds. It participates in the synthesis of ω-chain shortened prostaglandins.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis of a Prostaglandin Intermediate and Synthesis of Dihydrojasmone and Methyl Dihydrojasmonate.
Naoshima Y, et al.
Agricultural and Biological Chemistry, 43(8), 1765-1768 (1979)
Siham El Fangour et al.
Age (Dordrecht, Netherlands), 31(4), 269-276 (2009-05-30)
Oxidative damage from reactive oxygen species (ROS) and the carbon-centred radicals arising from them is important to the process of aging, and age-related diseases are generally caused, exacerbated or mediated by oxidative stress. Nitrones can act as spin traps to
David J Hart
Organic Synthesis via Examination of Selected Natural Products, 99-99 null
Synthesis of ω-chain shortened prostaglandins and their six-membered ring analogs.
Naoshima Y, et al.
Agricultural and Biological Chemistry, 48(3), 783-787 (1984)
Cinzia B Botta et al.
Journal of medicinal chemistry, 54(7), 2165-2182 (2011-03-23)
Several oxime containing molecules, characterized by a SAHA-like structure, were explored to select a potentially new biasing binding element for the zinc in HDAC catalytic site. All compounds were evaluated for their in vitro inhibitory activity against the 11 human

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