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(MESITYLAMINO)(OXO)ACETIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79354-46-4

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79354-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79354-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,5 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79354-46:
(7*7)+(6*9)+(5*3)+(4*5)+(3*4)+(2*4)+(1*6)=164
164 % 10 = 4
So 79354-46-4 is a valid CAS Registry Number.

79354-46-4Downstream Products

79354-46-4Relevant academic research and scientific papers

Visible-light mediated carbamoyl radical addition to heteroarenes

Jatoi, Ashique Hussain,Pawar, Govind Goroba,Robert, Frédéric,Landais, Yannick

, p. 466 - 469 (2019/01/10)

The generation of carbamoyl radicals, followed by their addition to heteroarenes, was performed under mild conditions through a metal-free photocatalyzed decarboxylation of oxamic acids. The process has been applied to the carbamoylation of heteroaromatic bases using α-aminoacid-derived oxamic acids, leading to the corresponding amides without racemization.

Improved microwave synthesis of unsymmetrical N,N'-diaryl-1,2-aminoethane and imidazolidinium salts as precursors of N-heterocyclic carbenes

Ibrahim, Yehia A.,Al-Awadi, Nouria A.,Al-Azemi, Talal F.,John, Elizabeth

, p. 38869 - 38876 (2014/11/08)

Lithium aluminium hydride reduction of bis-unsymmetric-diaryloxamides 3 is difficult to accomplish especially for the sterically hindered mesityl derivative. Using microwaves LAH reduction of 3a,d was successful in a short time, however, with cleavage of the ether linkage to give compounds 11a,d. Extension of this method enabled the reduction of bis-oxamide derivatives 13 to the corresponding tetraamine derivative 14 which was then converted to the bis-imidazolidinium salt 15. Application of this method led to rapid reduction of unsymmetric N,N'-diaryloxamides 16 to the corresponding N,N'- diarylethylenediamines 17 which were converted to their corresponding imidazolidinium salts 18. the Partner Organisations 2014.

Synthesis of amino acid derived imidazolidinium salts as new NHC precatalysts

Strand, Ragnhild B.,Helgerud, Trygve,Solvang, Tina,Sperger, Christian A.,Fiksdahl, Anne

, p. 1994 - 2006 (2012/03/22)

The preparation of new chiral symmetrically and unsymmetrically N,N′-disubstituted imidazolium based NHC salts Ib, IIb, IIIa-c and IVc-h from the amino acids l-proline and l-phenylalanine, is reported. Some preliminary tests have been carried out, demonstrating that the chiral NHCs give chiral induction in organometallic catalysis and can be used as organocatalysts.

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