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[ CAS No. 6270-63-9 ] {[proInfo.proName]}

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Chemical Structure| 6270-63-9
Chemical Structure| 6270-63-9
Structure of 6270-63-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 6270-63-9 ]

CAS No. :6270-63-9 MDL No. :MFCD11877813
Formula : C4H4N2O Boiling Point : No data available
Linear Structure Formula :- InChI Key :HUTNOYOBQPAKIA-UHFFFAOYSA-N
M.W : 96.09 Pubchem ID :72758
Synonyms :

Calculated chemistry of [ 6270-63-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 24.86
TPSA : 45.75 ?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) : -7.94 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.75
Log Po/w (XLOGP3) : -1.49
Log Po/w (WLOGP) : -0.23
Log Po/w (MLOGP) : -1.08
Log Po/w (SILICOS-IT) : 1.24
Consensus Log Po/w : -0.16

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.13
Solubility : 71.0 mg/ml ; 0.739 mol/l
Class : Very soluble
Log S (Ali) : 1.03
Solubility : 1040.0 mg/ml ; 10.8 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -1.47
Solubility : 3.23 mg/ml ; 0.0337 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.74

Safety of [ 6270-63-9 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H302-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 6270-63-9 ]

* 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 [ 6270-63-9 ]

[ 6270-63-9 ] Synthesis Path-Upstream   1~15

  • 1
  • [ 5049-61-6 ]
  • [ 6270-63-9 ]
YieldReaction ConditionsOperation in experiment
53% at 0 - 40℃; for 1 h; Sodium nitrite (3.4 g, 50 mmol, 1.3 eq.) was added in small portionsto 98percent sulfuric acid (15 mL) ice bath, and the mixture was allowed towarm up and heated to 60. When getting clear, the solution wascooled in an ice bath again. A solution of 2-amino-pyrazine (9) (4 g,39.3 mmol, 1 eq.) in 98percent sulfuric acid (15 mL) was added dropwise.The reaction mixture was stirred at 40 for 1 h. After cooling to roomtemperature, it was slowly poured onto crushed ice and stirred until nonitrogen run out. The solution was adjusted to pH 6 with a 40percent solutionof sodium hydroxide, resulting in lots of sodium sulfate which wasfiltered off whereafter. The filtrate was extracted with EA (50 mL×3),and the combined organics were dried (Na2SO4), filtered and concentratedin vacuo to give the product as a white precipitate (6.38 g,53percent).
Reference: [1] Bioorganic and Medicinal Chemistry, 2019, vol. 27, # 5, p. 748 - 759
[2] Journal of the Chemical Society, 1947, p. 371
[3] Journal of the American Chemical Society, 1946, vol. 68, p. 400
[4] Journal of Biological Chemistry, 1947, vol. 171, p. 321,324
  • 2
  • [ 131543-46-9 ]
  • [ 1668-10-6 ]
  • [ 6270-63-9 ]
Reference: [1] Journal of the American Chemical Society, 1952, vol. 74, p. 1580,1582
[2] Journal of the American Chemical Society, 1949, vol. 71, p. 78,79, 80
  • 3
  • [ 14508-49-7 ]
  • [ 6270-63-9 ]
Reference: [1] Journal of the American Chemical Society, 1946, vol. 68, p. 400
  • 4
  • [ 290-37-9 ]
  • [ 6270-63-9 ]
Reference: [1] Tetrahedron, 1995, vol. 51, # 43, p. 11855 - 11862
  • 5
  • [ 98197-78-5 ]
  • [ 6270-63-9 ]
Reference: [1] Heterocycles, 1989, vol. 28, # 1, p. 249 - 258
  • 6
  • [ 290-37-9 ]
  • [ 873-67-6 ]
  • [ 6270-63-9 ]
Reference: [1] Tetrahedron, 1995, vol. 51, # 43, p. 11855 - 11862
  • 7
  • [ 131543-46-9 ]
  • [ 6011-14-9 ]
  • [ 6270-63-9 ]
Reference: [1] Patent: US2805223, 1955, ,
  • 8
  • [ 70090-33-4 ]
  • [ 6270-63-9 ]
  • [ 111-66-0 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984, # 4, p. 641 - 646
  • 9
  • [ 149280-95-5 ]
  • [ 6270-63-9 ]
Reference: [1] Heterocycles, 1996, vol. 43, # 4, p. 883 - 889
[2] Heterocycles, 1996, vol. 43, # 4, p. 883 - 889
  • 10
  • [ 90862-01-4 ]
  • [ 6270-63-9 ]
  • [ 103-30-0 ]
  • [ 35684-26-5 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984, # 4, p. 641 - 646
  • 11
  • [ 38028-67-0 ]
  • [ 6270-63-9 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1986, p. 1255 - 1258
  • 12
  • [ 70090-29-8 ]
  • [ 6270-63-9 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984, # 4, p. 641 - 646
  • 13
  • [ 65032-05-5 ]
  • [ 6270-63-9 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984, # 4, p. 641 - 646
  • 14
  • [ 70090-30-1 ]
  • [ 6270-63-9 ]
  • [ 74-85-1 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1986, p. 1585 - 1588
  • 15
  • [ 65032-05-5 ]
  • [ 6270-63-9 ]
  • [ 74-85-1 ]
Reference: [1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1986, p. 1585 - 1588
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