10499-33-9 Usage
General Description
(NE)-N-(2-chlorocyclooctylidene)hydroxylamine is a chemical compound with the molecular formula C8H15ClNO. It is classified as an organic hydroxylamine which contains a cyclooct-3-en-1-ylidene group and a chlorine atom attached to the cyclooctene ring. (NE)-N-(2-chlorocyclooctylidene)hydroxylamine has the potential to act as a radical scavenger and has been studied for its antioxidant properties. Furthermore, (NE)-N-(2-chlorocyclooctylidene)hydroxylamine is also known for its potential as an anti-inflammatory and anti-cancer agent. Its molecular structure and properties make it a promising candidate for further research and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10499-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,9 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10499-33:
(7*1)+(6*0)+(5*4)+(4*9)+(3*9)+(2*3)+(1*3)=99
99 % 10 = 9
So 10499-33-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H14ClNO/c9-7-5-3-1-2-4-6-8(7)10-11/h7,11H,1-6H2/b10-8-
10499-33-9Relevant articles and documents
Oxidation of gem-chloronitroso- and vic-chloronitroso-alkanes and -cycloalkanes to respective chloronitro compounds by novel cetyltrimethylammonium hypochlorite reagent
Mohammed, Abdulkarim H.A.,Nagendrappa, Gopalpur
experimental part, p. 433 - 441 (2012/03/26)
Cetyltrimethylammonium hypochlorite (CTAHC) is prepared and used as an oxidizing agent for nitroso group to nitro group. The gem-chloronitroso and vic-chloronitroso compounds are prepared respectively from ketoximes and olefins by reacting with NOCl generated in situ from chlorotrimethylsilane (TMSC1 (l) and iso-amyl nitrite. CTAHC oxidizes gem-chloronitroso and vic-chloronitroso compounds to the corresponding chloronitro derivatives. While gem-chloronitro compounds are obtained in good yields, the vic-chloronitro derivatives are formed in moderate yields, because of the propensity of the vic-chloronitroso group to tautomerize to α-chlorooxime. The present method is simple and practical, particularly for the preparation of vic-chloronitro compounds, considering the fact that the known methods of their preparation are few and quite involved. Indian Academy of Sciences.
