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Merck

136948

Sigma-Aldrich

5-壬酮

98%

别名:

二丁基甲酮, 二异丁基酮

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About This Item

线性分子式:
CH3(CH2)3CO(CH2)3CH3
CAS号:
分子量:
142.24
Beilstein:
1743583
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

liquid

折射率

n20/D 1.419 (lit.)

bp

186-187 °C (lit.)

mp

−50 °C (lit.)

密度

0.826 g/mL at 25 °C (lit.)

官能基

ketone

SMILES 字串

CCCCC(=O)CCCC

InChI

1S/C9H18O/c1-3-5-7-9(10)8-6-4-2/h3-8H2,1-2H3

InChI 密鑰

WSGCRAOTEDLMFQ-UHFFFAOYSA-N

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應用

5-Nonanone can be used as a reactant to prepare:
  • 5-nonanketoxime by reacting with hydroxylamine in water.
  • 4-Nitro-2,6-dipropylphenol by treating with a solution of formyl nitroenamine in the presence of a base.

生化/生理作用

5-Nonanone induces clinical neuropathy in rats.

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

141.8 °F - closed cup

閃點(°C)

61 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

Lot/Batch Number

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Development of a general Pd (II)-catalyzed intermolecular hydroalkoxylation reaction of vinylphenols by using a sacrificial alcohol as the hydride source
Zhang Y and Sigman MS
Organic Letters, 8(24), 5557-5560 (2006)
Techno-economic analysis of 5-nonanone production from levulinic acid.
Patel AD, et al.
Chemical Engineering Journal, 160(1), 311-321 (2010)
Controlling selectivity in the reaction network of aldoxime hydrogenation to primary amines
Gebauer-Henke E, et al.
Catalysis Science & Technology, 2(12), 2539-2548 (2012)
Controlling Selectivity in the Consecutive Reaction Network of Aldoxime Hydrogenation to Primary Amines.
Gebauer-Henke E, et al.
Catalysis Science & Technology, 2, 2539-2548 (2012)
A convenient method for synthesizing modified 4-nitrophenols
Nakaike Y, et al.
The Journal of Organic Chemistry, 70(24), 10169-10171 (2005)

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