D187208
2,5-二甲基四氢呋喃（顺反异构体混合物）
96%
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关于此项目
经验公式（希尔记法）:
C6H12O
化学文摘社编号:
分子量:
100.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-707-6
Beilstein/REAXYS Number:
102563
MDL number:
Assay:
96%
Form:
liquid
Quality Level
assay
96%
form
liquid
refractive index
n20/D 1.404 (lit.)
bp
90-92 °C (lit.)
density
0.833 g/mL at 25 °C (lit.)
SMILES string
CC1CCC(C)O1
InChI
1S/C6H12O/c1-5-3-4-6(2)7-5/h5-6H,3-4H2,1-2H3
InChI key
OXMIDRBAFOEOQT-UHFFFAOYSA-N
John M Simmie
The journal of physical chemistry. A, 116(18), 4528-4538 (2012-04-13)
The enthalpies of formation, entropies, specific heats at constant pressure, enthalpy functions, and all carbon-hydrogen and carbon-methyl bond dissociation energies have been computed using high-level methods for the cyclic ethers (oxolanes) tetrahydrofuran, 2-methyltetrahydrofuran, and 2,5-dimethyltetrahydrofuran. Barrier heights for hydrogen-abstraction reactions
A S Anderson et al.
The Journal of organic chemistry, 65(15), 4648-4654 (2000-08-26)
2'-Deoxy-5-methyleneuridin-5-yl (1) is produced in a variety of DNA damage processes and is believed to result in the formation of lesions that are mutagenic and refractory to enzymatic repair. 2'-Deoxy-5-methyleneuridin-5-yl (1) was independently generated under anaerobic conditions via Norrish Type
M S Akhlaq et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 51(1), 91-102 (1987-01-01)
Thiyl radicals (RS) formed by the reaction of radiolytically generated OH radicals with thiols, e.g. 1,4-dithiothreitol (DTT), react with cis- and trans-2,5-dimethyltetrahydrofuran by abstracting an H atom in the alpha-position to the ether function (k approximately equal to 5 X
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| D187208-5G | 04061837717048 |
| D187208-100G | 04061837715785 |