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Merck
CN

D251

Sigma-Aldrich

十氢萘,顺式和反式的混合物

reagent grade, 98%

别名:

Decalin

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About This Item

经验公式(希尔记法):
C10H18
CAS号:
分子量:
138.25
Beilstein:
878165
EC 号:
MDL编号:
UNSPSC代码:
12352001
PubChem化学物质编号:
NACRES:
NA.21
等级:
reagent grade
方案:
98%
沸点:
189-191 °C (lit.)
蒸汽压:
42 mmHg ( 92 °C)
741 mmHg ( 188 °C)

等级

reagent grade

质量水平

蒸汽密度

4.76 (vs air)

蒸汽压

42 mmHg ( 92 °C)
741 mmHg ( 188 °C)

方案

98%

表单

liquid

自燃温度

482 °F

expl. lim.

0.7-4.9 %, 100 °F

折射率

n20/D 1.474 (lit.)

沸点

189-191 °C (lit.)

mp

−125 °C (lit.)

密度

0.896 g/mL at 25 °C (lit.)

SMILES字符串

C1CCC2CCCCC2C1

InChI

1S/C10H18/c1-2-6-10-8-4-3-7-9(10)5-1/h9-10H,1-8H2

InChI key

NNBZCPXTIHJBJL-UHFFFAOYSA-N

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一般描述

Decahydronaphthalene, mixture of cis + trans is a bicyclic organic compound that can be used as an industrial solvent. It can be prepared by the complete catalytic hydrogenation of naphthalene or tetralin.

应用

Decahydronaphthalene, mixture of cis+ trans can be used as a solvent in the:
  • Distannoxane-catalyzed synthesis of aliphatic polyesters via polycondensation.
  • Intramolecular carbonyl-ene cyclocondensation of oxygenated o-phenylallylbenzaldehydes to synthesize substituted naphthalenes.

法律信息

Decalin is a trademark of Sigma-Aldrich Co. LLC

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1C

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

134.6 °F - closed cup

闪点(°C)

57 °C - closed cup

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ken K Qian et al.
Journal of pharmaceutical sciences, 100(7), 2801-2815 (2011-02-22)
Spontaneous crystalline-to-amorphous phase transformation of organic or medicinal molecules in the presence of mesoporous materials has been observed, for which pathway was suggested to be via the vapor phase, that is, sublimation of the crystalline molecules followed by adsorption on
Mohit Kumar et al.
Nanoscale, 3(5), 2130-2133 (2011-03-30)
Naphthalene diimide (NDI) bolaamphiphilic molecules (1) self-assemble in water to form organic nanoparticles, which exhibit self-assembly induced preassociated excimer formation and hence an enhanced green fluorescence.
Sabir Hussain et al.
Journal of the American Chemical Society, 133(6), 1614-1617 (2011-01-25)
Decalins bearing two axial -NHCONHAr substituents and an ester-linked alkyl side chain have been synthesized and studied as anion receptors and transporters. The design relates to steroid-based "cholapods" but is more compact and less intrinsically lipophilic. Transport rates depend on
Sylvie Goncalves et al.
The Journal of organic chemistry, 76(9), 3274-3285 (2011-03-31)
An unprecedented and highly diastereoselective 6-endo-trig cyclization of 2-alkenyl-1,3-dithiolanes has been developed yielding trans-decalins, an important scaffold present in numerous di- and triterpenes. The novelty of this 6-endo-trig cyclization stands in the stepwise mechanism involving 2-alkenyl-1,3-dithiolane, acting as a novel
Shaik Anwar et al.
Organic letters, 13(9), 2200-2203 (2011-04-12)
An efficient and unprecedented organocatalytic reaction of γ-nitroketones with α,β-unsaturated aldehydes to give polyfunctionalized [4.4.0] bicyclic skeletons was developed. The diphenylprolinol silyl ether mediated nitro-Michael/Aldol reaction afforded the hexa-substituted decalin carboaldehydes with excellent diastereo- and enantioselectivity (up to >99:1 dr

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