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N-(2,5-dimethyl-4-oxocyclohexa-2,5-dien-1-ylidene)-N'-(phenylsulfonyl)benzenecarboximidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

461672-48-0

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461672-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 461672-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,1,6,7 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 461672-48:
(8*4)+(7*6)+(6*1)+(5*6)+(4*7)+(3*2)+(2*4)+(1*8)=160
160 % 10 = 0
So 461672-48-0 is a valid CAS Registry Number.

461672-48-0Relevant articles and documents

Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XIV.* halogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5- dialkyl-1,4-benzoquinone monoimines and their reduction products

Avdeenko,Konovalova,Ledeneva,Santalova,Pirozhenko,Palamarchuk,Shishkin

, p. 928 - 937 (2012/11/07)

Despite steric hindrances created by the bulky substituent on the nitrogen atom, halogenation of 2,5-dialkyl-N-[arylsulfonylimino(phenyl)methyl]-1,4- benzoquinone monoimines fairly readily gives their derivatives having two halogen atoms in the quinoid ring. Pleiades Publishing, Ltd., 2012.

Hydrohalogenation of N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinone monoimines having alkyl substituents in the quinoid ring

Avdeenko,Konovalova,Pirozhenko,Ledeneva,Santalova

experimental part, p. 1035 - 1044 (2011/11/14)

Hydrohalogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5(3,5)-dimethyl- 1,4-benzoquinone monoimines follows exclusively the 1,4-addition pattern, whereas N-[arylsulfonylimino(phenyl)methyl]-2,6-dimethyl-1,4-benzoquinone monoimines take up hydrogen halides according to the 6,3-addition scheme.

Thiocyanation of N-arylsulfonyl-, N-aroyl-, and N-[(N-arylsulfonyl) benzimidoyl]-1,4-benzoquinone imines

Avdeenko,Pirozhenko,Konovalov,Roman'Kov,Palamarchuk,Shishkinc

experimental part, p. 408 - 416 (2009/09/06)

Reactions of thiocyanate ion with N-aroyl-, N-arylsulfonyl-, and N-(N-arylsulfonylbenzimidoyl)-1,4-benzoquinone imines follow the 1,4-addition pattern, and the adducts undergo intramolecular cyclization to give the corresponding N-substituted 5-amino-1,3-

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