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[ CAS No. 21279-64-1 ] {[proInfo.proName]}

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Chemical Structure| 21279-64-1
Chemical Structure| 21279-64-1
Structure of 21279-64-1 * Storage: {[proInfo.prStorage]}

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Product Citations

Product Citations

Gregory R. Armel ; James T. Brosnan ; Nilda R. Burgos , et al. DOI:

Abstract: Numerous similarities exist between the structure–activity relationships of pharmaceutical drugs and pesticides, creating the potential for finding new crop management tools with novel mechanisms of action. Analogues of pyrazinamide and its active metabolite pyrazinoic acid were evaluated on a variety of monocot and dicot species to assess their potential as commercial herbicides. Six analogues, applied postemergence at 3 kg ai/ha, controlled yellow nutsedge (Cyperus esculentus) ≥ the commercial standards bentazon or imazethapyr. The compound 5-fluoropyrazine-2-carboxylic acid provided between 71 and 95% control of barnyardgrass (Echinochloa crus-galli) and yellow nutsedge with only modest injury (8–25%) to soybean (Glycine max). A similar compound containing a bromine atom in the 5-position controlled yellow nutsedge greater than bentazon and affected soybean, sweet corn (Zea mays convar. saccharata var. rugosa), and rice (Oryza sativa) in a similar fashion to bentazon as well. The herbicidal sites of action targeted by these analogues of pyrazinamide and pyrazinoic acid are unknown, but it is hypothesized that they may be disrupting targets in the biosynthesis pathways of nicotinamide adenine dinucleotide (NAD) and/or ethylene.

Keywords: herbicide ; rice ; pyrazinamide ; pharmaceutical ; prodrug ; soybean ; sweet corn

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Product Details of [ 21279-64-1 ]

CAS No. :21279-64-1 MDL No. :MFCD10686873
Formula : C5H4ClN3O Boiling Point : -
Linear Structure Formula :- InChI Key :GFEFMHWOSWUJSO-UHFFFAOYSA-N
M.W : 157.56 Pubchem ID :181450
Synonyms :

Calculated chemistry of [ 21279-64-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 35.14
TPSA : 68.87 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.06
Log Po/w (XLOGP3) : -0.51
Log Po/w (WLOGP) : 0.23
Log Po/w (MLOGP) : -1.01
Log Po/w (SILICOS-IT) : 0.73
Consensus Log Po/w : 0.1

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.87
Solubility : 21.1 mg/ml ; 0.134 mol/l
Class : Very soluble
Log S (Ali) : -0.47
Solubility : 53.6 mg/ml ; 0.34 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.84
Solubility : 2.25 mg/ml ; 0.0143 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.84

Safety of [ 21279-64-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 21279-64-1 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 21279-64-1 ]
  • Downstream synthetic route of [ 21279-64-1 ]

[ 21279-64-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 14508-49-7 ]
  • [ 77287-34-4 ]
  • [ 21279-62-9 ]
  • [ 36070-79-8 ]
  • [ 21279-64-1 ]
Reference: [1] Collection of Czechoslovak Chemical Communications, 1990, vol. 55, # 10, p. 2493 - 2501
[2] Collection of Czechoslovak Chemical Communications, 1990, vol. 55, # 10, p. 2493 - 2501
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