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[ CAS No. 20662-84-4 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
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Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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3d Animation Molecule Structure of 20662-84-4
Chemical Structure| 20662-84-4
Chemical Structure| 20662-84-4
Structure of 20662-84-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 20662-84-4 ]

CAS No. :20662-84-4 MDL No. :MFCD00005308
Formula : C6H9NO Boiling Point : -
Linear Structure Formula :- InChI Key :ZRLDBDZSLLGDOX-UHFFFAOYSA-N
M.W : 111.14 Pubchem ID :30215
Synonyms :

Calculated chemistry of [ 20662-84-4 ]

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.5
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 31.4
TPSA : 26.03 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.98
Log Po/w (XLOGP3) : 1.54
Log Po/w (WLOGP) : 1.6
Log Po/w (MLOGP) : 0.32
Log Po/w (SILICOS-IT) : 2.13
Consensus Log Po/w : 1.51

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.96
Solubility : 1.21 mg/ml ; 0.0109 mol/l
Class : Very soluble
Log S (Ali) : -1.7
Solubility : 2.24 mg/ml ; 0.0201 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.34
Solubility : 0.509 mg/ml ; 0.00458 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.29

Safety of [ 20662-84-4 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P403+P235 UN#:1993
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 20662-84-4 ]

* 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 [ 20662-84-4 ]
  • Downstream synthetic route of [ 20662-84-4 ]

[ 20662-84-4 ] Synthesis Path-Upstream   1~16

  • 1
  • [ 19322-27-1 ]
  • [ 52-90-4 ]
  • [ 3581-91-7 ]
  • [ 74015-70-6 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 2001, vol. 49, # 2, p. 816 - 822
  • 2
  • [ 141118-45-8 ]
  • [ 20662-84-4 ]
Reference: [1] Tetrahedron Letters, 1990, vol. 31, # 14, p. 1945 - 1948
[2] Journal of Organic Chemistry, 1992, vol. 57, # 12, p. 3331 - 3336
  • 3
  • [ 6628-81-5 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of Organic Chemistry, 1947, vol. 12, p. 43,45
[2] Journal of the American Chemical Society, 1948, vol. 70, p. 2005[3] Organic Syntheses, 1953, vol. 33, p. 1
[4] Chemische Berichte, 1951, vol. 84, p. 96,99
[5] Journal of the American Chemical Society, 1969, vol. 91, p. 4749 - 4760
[6] Yakugaku Zasshi, 1960, vol. 80, p. 895 - 901
  • 4
  • [ 42105-25-9 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1989, vol. 26, p. 269 - 275
  • 5
  • [ 10341-63-6 ]
  • [ 75-36-5 ]
  • [ 20662-84-4 ]
Reference: [1] Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1981, vol. <B> 20, # 4, p. 322 - 323
  • 6
  • [ 10341-59-0 ]
  • [ 20662-84-4 ]
Reference: [1] Tetrahedron Letters, 1980, vol. 21, p. 2359 - 2360
  • 7
  • [ 513-86-0 ]
  • [ 20662-84-4 ]
  • [ 22694-96-8 ]
  • [ 1124-11-4 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 1997, vol. 45, # 5, p. 1878 - 1882
  • 8
  • [ 134536-78-0 ]
  • [ 20662-84-4 ]
  • [ 3145-91-3 ]
Reference: [1] Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1991, # 2, p. 307 - 314
  • 9
  • [ 134536-78-0 ]
  • [ 16887-00-6 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999), 1991, # 2, p. 307 - 314
  • 10
  • [ 75-05-8 ]
  • [ 78-93-3 ]
  • [ 20662-84-4 ]
Reference: [1] Chemistry Letters, 1983, p. 1355 - 1356
[2] Chemistry Letters, 1983, p. 1355 - 1356
  • 11
  • [ 108-24-7 ]
  • [ 302-72-7 ]
  • [ 20662-84-4 ]
Reference: [1] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1933, vol. 218, p. 129,138
  • 12
  • [ 6628-81-5 ]
  • [ 7664-93-9 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of the American Chemical Society, 1948, vol. 70, p. 2006
  • 13
  • [ 19322-27-1 ]
  • [ 52-90-4 ]
  • [ 3581-91-7 ]
  • [ 74015-70-6 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of Agricultural and Food Chemistry, 2001, vol. 49, # 2, p. 816 - 822
  • 14
  • [ 60-35-5 ]
  • [ 814-75-5 ]
  • [ 20662-84-4 ]
Reference: [1] Chemische Berichte, 1953, vol. 86, p. 96,107
[2] Chemische Berichte, 1953, vol. 86, p. 96,107
  • 15
  • [ 127-09-3 ]
  • [ 108-24-7 ]
  • [ 302-72-7 ]
  • [ 20662-84-4 ]
Reference: [1] Journal of Organic Chemistry, 1947, vol. 12, p. 43,45
[2] Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, 1933, vol. 218, p. 129,138
  • 16
  • [ 20662-84-4 ]
  • [ 13623-11-5 ]
Reference: [1] Zhurnal Obshchei Khimii, 1958, vol. 28, p. 7,10; engl. Ausg. S. 5, 7
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