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67363-26-2

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67363-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67363-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,6 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67363-26:
(7*6)+(6*7)+(5*3)+(4*6)+(3*3)+(2*2)+(1*6)=142
142 % 10 = 2
So 67363-26-2 is a valid CAS Registry Number.

67363-26-2Relevant articles and documents

Chemical intervention in bacterial lignin degradation pathways: Development of selective inhibitors for intradiol and extradiol catechol dioxygenases

Sainsbury, Paul D.,Mineyeva, Yelena,Mycroft, Zoe,Bugg, Timothy D.H.

, p. 102 - 109 (2015)

Bacterial lignin degradation could be used to generate aromatic chemicals from the renewable resource lignin, provided that the breakdown pathways can be manipulated. In this study, selective inhibitors of enzymatic steps in bacterial degradation pathways

Photoinduced Aerobic Iodoarene-Catalyzed Spirocyclization of N-Oxy-amides to N-Fused Spirolactams**

Cariou, Kevin,Habert, Lo?c

supporting information, p. 171 - 175 (2020/10/27)

Iodoarene catalysis is a powerful methodology that usually requires an excess of oxidant, or of redox mediator if the terminal oxidant is dioxygen, to generate the key hypervalent iodine intermediate to proceed efficiently. We report that, using the spiro-cyclization of amides as a benchmark reaction, aerobic iodoarene catalysis can be enabled by relying on a pyrylium photocatalyst under blue light irradiation. This unprecedented dual organocatalytic system allows the use of low catalytic loading of both catalysts under very mild operating conditions.

Cross metathesis-mediated synthesis of hydroxamic acid derivatives

Chattopadhyay, Shital Kumar,Ghosh, Subhankar,Sil, Suman

, p. 3070 - 3075 (2019/01/05)

An alternative synthesis of α,?-unsaturated hydroxamates via cross metathesis between a class-I olefin and N-benzyloxyacrylamide is reported. The reaction proceeds better in the presence of Grubbs' second generation catalyst within short time and in good

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