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[ CAS No. 101935-40-4 ] {[proInfo.proName]}

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Chemical Structure| 101935-40-4
Chemical Structure| 101935-40-4
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Product Details of [ 101935-40-4 ]

CAS No. :101935-40-4 MDL No. :MFCD08704555
Formula : C6H4BrNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :HRVRWIBVVHOHNN-UHFFFAOYSA-N
M.W : 218.01 Pubchem ID :8167254
Synonyms :

Calculated chemistry of [ 101935-40-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
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 : 44.99
TPSA : 66.05 ?2

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) : 1.31
Log Po/w (XLOGP3) : 2.09
Log Po/w (WLOGP) : 2.06
Log Po/w (MLOGP) : 1.05
Log Po/w (SILICOS-IT) : -0.1
Consensus Log Po/w : 1.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.85
Solubility : 0.311 mg/ml ; 0.00143 mol/l
Class : Soluble
Log S (Ali) : -3.11
Solubility : 0.17 mg/ml ; 0.000782 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.06
Solubility : 1.89 mg/ml ; 0.00867 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.92

Safety of [ 101935-40-4 ]

Signal Word:Danger Class:9
Precautionary Statements:P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501 UN#:3077
Hazard Statements:H302-H315-H317-H318-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 101935-40-4 ]

* 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 [ 101935-40-4 ]
  • Downstream synthetic route of [ 101935-40-4 ]

[ 101935-40-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 101935-40-4 ]
  • [ 100367-36-0 ]
YieldReaction ConditionsOperation in experiment
43.9% With iron; acetic acid In ethanolReflux [00408] 2-Bromo-3-nitro-phenol (3.35 g, 15.4 mmol), acetic acid (35 mL) and iron powder(4.5 g, 77.2 mmol) were stirred in ethanol (50 mL) under reflux overnight. The mixture was diluted with 1 00m1 of water and neutralised with potassium carbonate before extraction with DCM. The organics were dried with sodium sulfate and concentrated in vacuo to leave the crude product as a brown oil. This was dry-packed on to silica and purified by columnchromatography using a 0-50percent gradient of ethyl acetate in isohexane. The resulting fragments were concentrated in vacuo to give 3-amino-2-bromo-phenol (1 .27 g, 6.75 mmol, 43.9percent) as a pale yellow solid.[00409] 1H NMR (DMSO-d6): O 7.02 (t, J = 8.0 Hz, 1H), 6.45 (dd, J= 1.6 and 8.0 Hz,1 H), 6.38 (dd, J = 1 .6 and 8.0 Hz, 1 H) 5.44 (bs, 1 H), 4.89 (bs, 2H).
Reference: [1] Journal of Organic Chemistry, 1988, vol. 53, # 6, p. 1170 - 1176
[2] Chemistry - A European Journal, 2017, vol. 23, # 42, p. 9996 - 10000
[3] Patent: WO2015/79251, 2015, A1, . Location in patent: Paragraph 00408; 00409
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