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35213-00-4

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35213-00-4 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 33, p. 434, 1990 DOI: 10.1021/jm00163a067The Journal of Organic Chemistry, 37, p. 3224, 1972 DOI: 10.1021/jo00986a007

Check Digit Verification of cas no

The CAS Registry Mumber 35213-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,1 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35213-00:
(7*3)+(6*5)+(5*2)+(4*1)+(3*3)+(2*0)+(1*0)=74
74 % 10 = 4
So 35213-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3N3O4/c8-4-5-2-1-3-6(9(11)12)7(5)10(13)14/h1-3H

35213-00-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L12624)  2,6-Dinitrobenzonitrile, 98+%   

  • 35213-00-4

  • 1g

  • 957.0CNY

  • Detail
  • Alfa Aesar

  • (L12624)  2,6-Dinitrobenzonitrile, 98+%   

  • 35213-00-4

  • 5g

  • 3997.0CNY

  • Detail

35213-00-4Relevant articles and documents

METHOD OF IMPROVING STABILITY OF SWEET ENHANCER AND COMPOSITION CONTAINING STABILIZED SWEET ENHANCER

-

, (2012/03/08)

The present invention includes methods of stabilizing one or more sweet enhancers when they are exposed to a light source as well as liquid compositions containing one or more sweet enhancers and one or more photostabilizers.

Antifolate and Antibacterial Activities of 5-Substituted 2,4-Diaminoquinazolines

Harris, Neil V.,Smith, Christopher,Bowden, Keith

, p. 434 - 444 (2007/10/02)

A series of 5-substituted 2,4-diaminoquinazolines (3) has been synthesized and evaluated as inhibitors of the enzyme dihydrofolate reductase (DHFR) from both bacterial and mammalian sources.The best compounds (e.g. 53) show good activity against Escherichia coli DHFR, but there is no significant selectivity for the bacterial over the mammalian enzyme.The structure-activity relationships for enzyme inhibition appear to be complex and not amenable to simple analysis; a hypotesis to explain the observed qualitative structure-activity relationships is proposed.The inhibitory activities of the compounds against the growth of intact bacterial cells in vitro closely parallel those for the inhibition of the isolated bacterial enzymes, suggesting that their antifolate action is responsible for their antibacterial effects.Five of the compounds were tested for their ability to cure a systemic E. coli infection in the mouse, but they showed no therapeutic effects at their maximum tolerated doses.

Derivatives of 4,6 dioxopyrido[3,2-g]quinoline 2,8 dicarboxylic acid

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, (2008/06/13)

Novel chemical compounds of the formula: SPC1 Wherein R is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, phenyl, alkali metal, or an amine cation; X and Y can be the same or different and are selected from the group consisting of hydrogen, alkyl of from one to six carbon atoms, inclusive, cycloalkyl of 5 or 6 carbon atoms, inclusive, phenyl, hydroxyl, alkoxy having from one to three carbon atoms, inclusive, halogen, trifluoromethyl, cyano, carboxyamide and O C-OQ, EQU1 where Q is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, alkali metal, and an amine cation, with the proviso that where R is hydrogen, alkali metal or an amine cation, then Q is the same as R, and where R is phenyl or alkyl from one to three carbon atoms, then Q is phenyl or alkyl from one to three carbon atoms; and Z is selected from the group consisting of hydrogen, alkyl from one to three carbon atoms, inclusive, and phenyl. The compounds are formulated with pharmaceutical carriers for oral or parenteral administration, with insufflation being the preferred method. The compositions are useful in the prophylactic treatment of sensitized humans and mammals for allergy and all anaphylactic reactions of a reagin or non-reagin mediated nature.

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