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Methylenebis(p-phenylene)diisocyanide, also known as MDI, is an organic compound widely used in the production of polyurethane polymers. It is a colorless, crystalline solid with the chemical formula C15H10N2O2. MDI is formed by the reaction of aniline with phosgene, resulting in a highly reactive molecule containing two isocyanate functional groups. Due to its high reactivity, MDI is used in the manufacture of flexible and rigid foams, elastomers, and coatings. It is also employed in the production of insulation materials, automotive parts, and various other industrial applications. However, it is important to note that MDI is a hazardous substance and requires proper handling and safety measures due to its potential health risks and environmental impact.

956-62-7

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956-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956-62-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 956-62:
(5*9)+(4*5)+(3*6)+(2*6)+(1*2)=97
97 % 10 = 7
So 956-62-7 is a valid CAS Registry Number.

956-62-7Relevant academic research and scientific papers

COMPOUNDS USEFUL IN HIV THERAPY

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Page/Page column 146, (2020/06/19)

The invention relates to compounds of Formula (I), (Ia), (Ib), (II) or (III), salts thereof, pharmaceutical compositions thereof, as well as therapeutic methods of treatment and prevention.

Iodide-Catalyzed Synthesis of Secondary Thiocarbamates from Isocyanides and Thiosulfonates

Mampuys, Pieter,Zhu, Yanping,Sergeyev, Sergey,Ruijter, Eelco,Orru, Romano V. A.,Van Doorslaer, Sabine,Maes, Bert U. W.

supporting information, p. 2808 - 2811 (2016/07/06)

A new method for the synthesis of secondary thiocarbamates from readily available isocyanides and thiosulfonates with broad functional group tolerance is reported. The reaction proceeds under mild reaction conditions in isopropanol and is catalyzed by inexpensive sodium iodide.

Synthesis and antiproliferative activity of aromatic and aliphatic bis[aminomethylidene(bisphosphonic)] acids

Goldeman, Waldemar,Nasulewicz-Goldeman, Anna

supporting information, p. 3475 - 3479 (2014/07/22)

A series of aromatic and aliphatic bis[aminomethylidene(bisphosphonic)] acids was synthesized in the reaction of triethylphosphite with isonitriles followed by hydrolysis or dealkylation. The in vitro anti-proliferative effect of all synthesized tetraphosphonic acids against MCF-7 breast cancer cells, J774E macrophages and HL-60 promyelocytic leukemia cells was determined. Three aromatic derivatives (5a, 5f and 5j) showed a similar or higher anti-proliferative activity than zoledronic acid.

Synthesis, characterization and mechanochromic behavior of binuclear gold (I) complexes with various diisocyano bridges

Liang, Jinhua,Hu, Fang,Lv, Xiaoyi,Chen, Zhao,Chen, Zhiming,Yin, Jun,Yu, Guang-Ao,Liu, Sheng Hua

, p. 485 - 490 (2012/10/30)

A series of binuclear gold (I) complexes were synthesized. Their structures were characterized by elemental analyses, IR spectrometry, UV-Vis spectroscopy and single crystal X-ray diffraction. Their fluorescent mechanochromic (tribochromic) properties were investigated. The results of the mechanochromic studies suggested that the gold complexes with methylsubstituted phenyl bridges exhibited mechanochromism and a 100 nm red-shift of fluorescent spectrum could be observed after grinding. The complex with a diphenylmethane bridge exhibited mechanochromism with a change in fluorescence from green to blue (25 nm red-shift after grinding). The ground complexes reverted to their original states by treatment with CH2Cl2. No mechanochromism was observed for either the biphenyl or diphenylethane containing complexes.

α-Thioxothioamides: A formal [4+1] cycloaddition reaction with isocyanides and diisocyanides and its application to a new straightforward formation of extended tetrathiafulvalenes

Morel, Georges,Marchand, Evelyne,Sinbandhit, Sourisak,Carlier, Roger

, p. 655 - 662 (2007/10/03)

A number of 2-(alkylimino) and 2-(arylimino)-l,3-dithioles (aza DTFs) bearing push-pull substituents have been prepared under mild conditions according to the title procedure. This novel strategy relies upon the fact that the use of conjugated diisocyanides allows an effective synthesis of new extended tetrathiafulvalenes (TTFs). The two dithiole moieties are linked by a conjugated framework that incorporates a phenyl, biphenyl or azobiphenyl group. High and low temperature measurements are required in order to understand the complex 1H and 13C NMR spectra of the prepared mono-bis- and tris-(1,3-dithiole) derivatives. Their electrochemical oxidations are also described.

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