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1089-82-3

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1089-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1089-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1089-82:
(6*1)+(5*0)+(4*8)+(3*9)+(2*8)+(1*2)=83
83 % 10 = 3
So 1089-82-3 is a valid CAS Registry Number.

1089-82-3Downstream Products

1089-82-3Relevant articles and documents

Deoxygenation Reactions of ortho-Nitrostyrenes with Carbon Monoxide Catalysed by Metal Carbonyls: a New Route to Indoles

Crotti, Corrado,Cenini, Sergio,Rindone, Bruno,Tollari, Stefano,Demartin, Francesco

, p. 784 - 786 (1986)

The metal carbonyls Fe(CO)5, Ru3(CO)12, and Rh6(CO)16 are catalysts for the deoxygenation of ortho-nitrostyrenes under carbon monoxide pressure to give indole derivatives; the crystal structure of a non-catalytically active rhodium complex obtained during the synthesis of (5e) is reported.

Nitrenium Ions. Part 1. Acid-catalysed Reactions of 2-Methylindole with Nitrosobenzenes. Crystal Structures of 2-Phenylamino-3-phenylimino-3H-indole, 2-(o-Tolylamino)-3-(o-tolylimino)-3H-indole, N-Phenyl-N-(2-phenylamino-3H-indol-3-ylidene)amine N-Oxide and Bis(2-methyl-1H-indol-3-yl)...

Cardellini, Liberato,Carloni, Patricia,Damiani, Elisabetta,Greci, Lucedio,Stipa, Pierluigi,et al.

, p. 1589 - 1596 (2007/10/02)

2-Methylindole 3b reacts with nitrosobenzenes 1a-c in the presence of monochloroacetic acid affording compounds which are characterized by the formation of carbon-nitrogen bonds and other compounds which clearly could arise from a radical mechanism.The radical component of the reaction is also supported by the EPR spectroscopy as well as the reaction products distribution.Although these reactions cannot be considered of synthetic value for the number of isolated products, they could be regarded as clear examples of the electrophilic character and of the oxidative power of nitrogen in activated nitrosobenzenes.Crystal structures of 2-phenylamino-3-phenylimino-3H-indole 7a, 2-(o-tolylamino)-3-(o-tolylimino)-3H-indole 7b, N-phenyl-N-(2-phenylamino-3H-indol-3-ylidene)amine N-oxide 9a and bis(2-methyl-1H-indol-3-yl)methane 10 are also reported.

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