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[ CAS No. 3400-55-3 ] {[proInfo.proName]}

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Chemical Structure| 3400-55-3
Chemical Structure| 3400-55-3
Structure of 3400-55-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 3400-55-3 ]

CAS No. :3400-55-3 MDL No. :MFCD00152299
Formula : C7H15BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :AHIUAFXWZKCJLR-UHFFFAOYSA-N
M.W : 211.10 Pubchem ID :103001
Synonyms :

Calculated chemistry of [ 3400-55-3 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.8
TPSA : 18.46 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) : -6.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.79
Log Po/w (XLOGP3) : 2.02
Log Po/w (WLOGP) : 2.17
Log Po/w (MLOGP) : 1.86
Log Po/w (SILICOS-IT) : 1.79
Consensus Log Po/w : 2.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.09
Solubility : 1.71 mg/ml ; 0.0081 mol/l
Class : Soluble
Log S (Ali) : -2.04
Solubility : 1.95 mg/ml ; 0.00923 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.29
Solubility : 1.09 mg/ml ; 0.00515 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 3.12

Safety of [ 3400-55-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P301+P312+P330-P302+P352-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 3400-55-3 ]

* 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 [ 3400-55-3 ]
  • Downstream synthetic route of [ 3400-55-3 ]

[ 3400-55-3 ] Synthesis Path-Upstream   1~6

  • 1
  • [ 17356-08-0 ]
  • [ 3400-55-3 ]
  • [ 7305-71-7 ]
Reference: [1] Yakugaku Zasshi, 1940, vol. 60, p. 433,439; dtsch. Ref. S. 219, 223[2] Chem.Abstr., 1941, p. 458
  • 2
  • [ 4744-08-5 ]
  • [ 3400-55-3 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1900, vol. 312, p. 289
[2] Journal of the American Chemical Society, 1951, vol. 73, p. 973
[3] Journal of the Chemical Society, 1925, vol. 127, p. 589
[4] Canadian Journal of Chemistry, 1971, vol. 49, p. 2321 - 2335
  • 3
  • [ 64-17-5 ]
  • [ 123-38-6 ]
  • [ 3400-55-3 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1971, vol. 751, p. 69 - 76
[2] Bulletin de la Societe Chimique de France, 1965, p. 2287 - 2295
[3] Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques, 1971, vol. 273, p. 418 - 421
[4] Journal of Organic Chemistry, 1961, vol. 26, p. 4183 - 4184
[5] Collection of Czechoslovak Chemical Communications, 1984, vol. 49, # 9, p. 2148 - 2166
  • 4
  • [ 123-38-6 ]
  • [ 3400-55-3 ]
Reference: [1] Journal of the Chemical Society, 1947, p. 371
[2] Journal of the Chemical Society, 1948, p. 41
  • 5
  • [ 56-23-5 ]
  • [ 128-08-5 ]
  • [ 4744-08-5 ]
  • [ 3400-55-3 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 973
  • 6
  • [ 603-35-0 ]
  • [ 3400-55-3 ]
  • [ 1530-32-1 ]
Reference: [1] Zeitschrift fuer Chemie (Stuttgart, Germany), 1968, vol. 8, p. 184
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