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[ CAS No. 61830-21-5 ] {[proInfo.proName]}

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Chemical Structure| 61830-21-5
Chemical Structure| 61830-21-5
Structure of 61830-21-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 61830-21-5 ]

CAS No. :61830-21-5 MDL No. :MFCD06669909
Formula : C6H7BrN2O2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :TWGNDRMYYDZGFI-UHFFFAOYSA-N
M.W : 251.10 Pubchem ID :1284665
Synonyms :

Calculated chemistry of [ 61830-21-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.33
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.3
TPSA : 93.45 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.28 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.98
Log Po/w (XLOGP3) : 2.18
Log Po/w (WLOGP) : 1.67
Log Po/w (MLOGP) : 0.63
Log Po/w (SILICOS-IT) : 2.23
Consensus Log Po/w : 1.74

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.88
Solubility : 0.331 mg/ml ; 0.00132 mol/l
Class : Soluble
Log S (Ali) : -3.78
Solubility : 0.0421 mg/ml ; 0.000168 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.27
Solubility : 1.34 mg/ml ; 0.00532 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.81

Safety of [ 61830-21-5 ]

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

Application In Synthesis of [ 61830-21-5 ]

* 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 [ 61830-21-5 ]

[ 61830-21-5 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 5398-36-7 ]
  • [ 61830-21-5 ]
YieldReaction ConditionsOperation in experiment
79% at 20 - 80℃; for 13.5 h; General procedure: 2-Aminothiazoles (0.1 mol) were dissolved in the least amount of glacial acetic acid, and then bromine (0.11 mol) was added drop-wise with continuous stirring at room temperature. The mixture was heated at 80 °C for 90 min then stirred at room temperature for 12 h. The mixture was filtered and washed with water. The precipitate was heated in water, and the aqueous solution was alkalized by ammonia, filtered, washed with water and then dried. Crystals were formed from ethanol/water to give the 5-bromothiazol-2-amine compounds 3a–f.
Reference: [1] Medicinal Chemistry Research, 2015, vol. 24, # 8, p. 3194 - 3211
[2] Journal of Medicinal Chemistry, 1977, vol. 20, p. 572 - 576
[3] Tetrahedron Letters, 2002, vol. 43, # 39, p. 7051 - 7053
[4] Patent: US2007/281979, 2007, A1, . Location in patent: Page/Page column 22
[5] Patent: US2007/4700, 2007, A1, . Location in patent: Page/Page column 23
  • 2
  • [ 5398-36-7 ]
  • [ 70-23-5 ]
  • [ 61830-21-5 ]
Reference: [1] Patent: US5705516, 1998, A,
  • 3
  • [ 70-23-5 ]
  • [ 61830-21-5 ]
Reference: [1] Medicinal Chemistry Research, 2015, vol. 24, # 8, p. 3194 - 3211
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