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700378-37-6

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700378-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 700378-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,3,7 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 700378-37:
(8*7)+(7*0)+(6*0)+(5*3)+(4*7)+(3*8)+(2*3)+(1*7)=136
136 % 10 = 6
So 700378-37-6 is a valid CAS Registry Number.

700378-37-6Downstream Products

700378-37-6Relevant articles and documents

β-sih-containing tris(silazido) rare-earth complexes as homogeneous and grafted single-site catalyst precursors for hydroamination

Eedugurala, Naresh,Wang, Zhuoran,Yan, Kaking,Boteju, Kasuni C.,Chaudhary, Umesh,Kobayashi, Takeshi,Ellern, Arkady,Slowing, Igor I.,Pruski, Marek,Sadow, Aaron D.

supporting information, p. 1142 - 1153 (2017/12/08)

A series of homoleptic rare-earth silazido compounds and their silica-grafted derivatives were prepared to compare spectroscopic and catalytic features under homogeneous and interfacial conditions. Trivalent tris-(silazido) compounds Ln{N(SiHMe2/sub

New highly active heteroscorpionate-containing lutetium catalysts for the hydroamination of aminoalkenes: Isolation and structural characterization of a dipyrrolidinide-lutetium complex

Otero, Antonio,Lara-Sanchez, Agustin,Najera, Carmen,Fernandez-Baeza, Juan,Marquez-Segovia, Isabel,Castro-Osma, Jose Antonio,Martinez, Javier,Sanchez-Barba, Luis F.,Rodriguez, Ana M.

scheme or table, p. 2244 - 2255 (2012/06/04)

The reactions of the hybrid scorpionate/cyclopentadiene compounds, as a mixture of regioisomers-1-[2,2-bis(3,5-dimethylpyrazol-1-yl)-1,1-diphenylethyl]- 1,3-cyclopentadiene and 2-[2,2-bis(3,5-dimethylpyrazol-1-yl)-1,1-diphenylethyl]- 1,3-cyclopentadiene (

Highly efficient, base-catalysed, intramolecular hydroamination of non-activated olefins

Quinet, Coralie,Jourdain, Pierre,Hermans, Christophe,Ates, Ali,Lucas, Isabelle,Markó, István E.

, p. 1077 - 1087 (2008/09/17)

The intramolecular hydroamination of a large variety of non-activated alkenes can be efficiently catalysed by small amounts of lithium bases, providing smoothly and in high yields the corresponding five- and six-membered ring heterocycles. Fused and bridged bicyclic amines, of varying ring sizes, can be readily prepared either by a sequential hydroamination process or by a tandem, double addition reaction.

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