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1026190-86-2

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1026190-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026190-86-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,1,9 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1026190-86:
(9*1)+(8*0)+(7*2)+(6*6)+(5*1)+(4*9)+(3*0)+(2*8)+(1*6)=122
122 % 10 = 2
So 1026190-86-2 is a valid CAS Registry Number.

1026190-86-2Relevant articles and documents

I2/CHP mediated [1 + 1 + 1 + 1] cyclization of aromatic isocyanides with amines to construct 1,3-diazetidine-2,4-diimine derivatives

Liu, Hai-Feng,Zhu, Tong-Hao,Xu, Pei,Wang, Shun-Yi,Ji, Shun-Jun

, p. 8738 - 8742 (2017)

An I2/CHP (cumene hydroperoxide) mediated [1 + 1 + 1 + 1] cyclization of aromatic isocyanides with readily accessible amines via the formation 4 new C-N bonds has been developed to construct unsymmetric 1,3-diazetidine-2,4-diimine derivatives u

Ultrasonic-assisted synthesis of carbodiimides from N,N′-disubstituted thioureas and ureas

Duangkamol, Chuthamat,Pattarawarapan, Mookda,Phakhodee, Wong

, p. 1945 - 1949 (2016/10/21)

A facile and efficient sonochemical method for the preparation of carbodiimides from their corresponding thioureas or ureas was described. Using Ph3P–I2 combination in the presence of triethylamine, various diaryl, aryl–alkyl, as well as dialkyl substituted substrates could be converted into carbodiimides in good-to-excellent yields within short reaction times under mild conditions with simple experimental setup. Graphical abstract: [Figure not available: see fulltext.]

The efficient synthesis of carbodiimides using a titanium imido complex

Anderson, James C.,Bou-Moreno, Rafael

experimental part, p. 9182 - 9186 (2011/01/12)

An efficient rt synthesis of carbodiimides or ureas from the combination of a titanium imido complex 2 and a range of 12 aryl and aliphatic isocyanates is described. Control experiments suggest that carbodimide formation is via heterocumulene metathesis t

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