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Tianjin Kind Pharma Co., Ltd.

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Tianjin Kind Pharma Co., Ltd.

Business Type:Lab/Research institutions

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Main Products:
Thiamidol,Bemotrizinol (Tinosorb S),Semaglutide,Lifitegrast,Risdiplam,Progesterone,PMK ethyl glycidate,Trilaciclib
Year Established:
2023
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Tianjin Kind Pharma Co., Ltd.

Country: China (Mainland)

Business Type:Lab/Research institutions

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Tel: +86-15510908448

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City: Tianjin

Street: No.22 Quanwang Road, Wuqing Development Zone, Tianjin, China

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CAS NO.314020-40-1

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  • 2-(2,6-Diethyl-4-Methylphenyl)malonamide
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The compound "2-(2,6-diethyl-4-methylphenyl)malonamide" is a malonamide derivative with the chemical formula C14H20N2O2 and a molecular weight of 248.32 g/mol. The IUPAC name for this compound is "2-(2,6-diethyl-4-methylphenyl)propanediamide."

Buy High Quality 2-(2,6-Diethyl-4-Methylphenyl)malonamide, Export 314020-40-1 with Efficient Delivery

2-(2,6-diethyl-4-methylphenyl): This part of the name indicates the substitution pattern on the phenyl ring. Specifically, there are two ethyl groups at positions 2 and 6, and a methyl group at position 4 on the phenyl ring.

malonamide: This indicates that the compound is a malonamide derivative. Malonamide is a compound derived from malonic acid.

References of 2-(2,6-Diethyl-4-Methylphenyl)malonamide 314020-40-1

The Synthesis of 2-(2,6-diethyl-4-methylphenyl)malonamide

CHEN Li-peng, LIAO Dao-hua, GAO Qian, LI Ai-jun, GUO Dong, YUE Hang, YANG Fan, Pharmacy School, East

China University of Science and Technology, 2014 Issue:  8

2,6-diethyl-4-methyl-bromobenzene was prepared from 2,6-diethyl-4-methylaniline by the Sandmeyer reaction, then coupled with malononitrile under palladium catalysis to give the 2,6-diethyl-4-methyl-phenyl-malononitrile, which was hydrolyzed to get the target product. The proposed synthetic route has many advantages, including high yield, easily available raw materials, few synthetic steps and it can be suitable for industrial production.

Attractive Interactions between Reverse Aggregates and Phase Separation in Concentrated Malonamide Extractant Solutions

C. Erlinger, L. Belloni, Th. Zemb, and C. Madic

Langmuir 1999, 15, 7, 2290–2300

Using small angle X-ray scattering, conductivity, and phase behavior determination, we show that concentrated solutions of molanamide extractants, dimethyldibutyltetradecylmalonamide (DMDBTDMA), are organized in reverse oligomeric aggregates which have many features in common with reverse micelles.