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411485

Sigma-Aldrich

丙二酸二异丙酯

ReagentPlus®, 99%

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About This Item

线性分子式:
(CH3)2CHO2CCH2CO2CH(CH3)2
CAS号:
13195-64-7
分子量:
188.22
EC號碼:
236-156-3
MDL號碼:
MFCD00059359
分類程式碼代碼:
12352100
PubChem物質ID:
24865749
NACRES:
NA.22

產品線

ReagentPlus®

化驗

99%

形狀

liquid

折射率

n20/D 1.412 (lit.)

bp

93-95 °C/12 mmHg (lit.)

密度

0.991 g/mL at 25 °C (lit.)

官能基

ester

SMILES 字串

CC(C)OC(=O)CC(=O)OC(C)C

InChI

1S/C9H16O4/c1-6(2)12-8(10)5-9(11)13-7(3)4/h6-7H,5H2,1-4H3

InChI 密鑰

QRVSDVDFJFKYKA-UHFFFAOYSA-N

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應用

Diisopropyl malonates may be used in the synthesis of :
  • 3-substituted coumarins
  • 2-carboisopropoxy-3-hydroxyquinoxaline-di-N-oxide
  • 2-carboisopropoxy-3-hydroxy-6-methoxylquinoxaline-di-N-oxide

法律資訊

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315,H319,H335

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

192.2 °F - closed cup

閃點（°C）

89 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
STBJ2912
STBG8765
STBB8099V
S37329V
STBB8099

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Use of isopropyl alcohol as a solvent in Ti (O-i-Pr) 4-catalyzed Knoevenagel reactions.
Yamashita K, et al.
Tetrahedron, 61(33), 7981-7985 (2005)
Yingjun Xu et al.
Molecules (Basel, Switzerland), 16(8), 6894-6901 (2011-08-16)
A series of quinoxaline 1,4-di-N-oxide analogues were prepared from benzofurazan N-oxide derivatives and β-diketone ester compounds by the improved Beirut reaction. The structures of the target products were characterized by NMR, MS, IR and elemental analysis measurements, and that of
A Catalytic Enantioselective Michael Addition of a Simple Malonate to Prochiral a, ?-Unsaturated Ketoses and Aldehydes.
Yamaguchi M, et al.
Angewandte Chemie (International Edition in English), 32(8), 1176-1178 (1993)
H Jinno et al.
Archives of toxicology, 71(9), 550-555 (1997-01-01)
The fungicide isoprothiolane (diisopropyl 1,3-dithiolane-2-ylidenemalonate) decomposes to the diisopropyl esters of malonic acid (DM), chloromalonic acid (DCM) and dichloromalonic acid (DDCM) upon aqueous chlorination. In this study, the cytotoxicity of these compounds was examined using rat hepatocytes cultured on Matrigel.

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