diethylbut-2-indioat

diethylbut-2-indioat Structure
diethylbut-2-indioat structure
Common Name diethylbut-2-indioat
CAS Number 762-21-0 Molecular Weight 170.163
Density 1.1±0.1 g/cm3 Boiling Point 233.9±0.0 °C at 760 mmHg
Molecular Formula C8H10O4 Melting Point 1-3 °C
MSDS Chinese USA Flash Point 94.4±0.0 °C
Symbol GHS05
GHS05
Signal Word Danger

Enhanced toxicity of the protein cross-linkers divinyl sulfone and diethyl acetylenedicarboxylate in comparison to related monofunctional electrophiles.

Chem. Res. Toxicol. 24(9) , 1457-9, (2011)

Previously, we determined that diethyl acetylenedicarboxylate (DAD), a protein cross-linker, was significantly more toxic than analogous monofunctional electrophiles. We hypothesized that other protein cross-linkers enhance toxicity similarly. In agreement wi...

3,4,5-Trisubstituted Furan-2(5H)-one Derivatives: Efficient one-pot Synthesis and Evaluation of Cytotoxic Activity.

Drug Res. (Stuttg.) , (2014)

A series of 3,4,5-trisubstituted 2(5H)-furanone derivatives was synthesized through one-pot reaction of amines, aldehydes and diethyl acetylenedicarboxylate. Silica sulfuric acid efficiently catalyzes the 3-component reaction to afford the corresponding 2(5H)...

Diels-Alder reactivity of polycyclic aromatic hydrocarbon bay regions: implications for metal-free growth of single-chirality carbon nanotubes.

J. Am. Chem. Soc. 131(44) , 16006-7, (2009)

A soluble bisanthene derivative, 4,11-dimesitylbisanthene, has been synthesized in three steps from bianthrone. In hot toluene, this bisanthene undergoes a clean Diels-Alder reaction with diethyl acetylenedicarboxylate to give a rearomatized 1:1 cycloadduct a...

Synthesis of novel highly functionalized 4-thiazolidinone derivatives from 4-phenyl-3-thiosemicarbazones.

Molecules 19(3) , 3068-83, (2014)

We present herein the synthesis in good yields of two series of highly functionalized thiazolidinone derivatives from the reactions of various 4-phenyl-3-thio-semicarbazones with ethyl 2-bromoacetate and diethyl acetylenedicarboxylate, respectively.

Synthesis of the anti-virus compound shuangkangsu's analogs.

J. Asian Nat. Prod. Res. 11(7) , 613-20, (2009)

Four novel cyclic peroxide glucosides 15a, 15b, 16a, and 16b, optically pure analogs of shuangkangsu (1), which is an anti-virus natural product with an unusual skeleton isolated from the buds of Lonicera japonica Thunb, were first synthesized totally in six ...