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[ CAS No. 38275-57-9 ] {[proInfo.proName]}

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Chemical Structure| 38275-57-9
Chemical Structure| 38275-57-9
Structure of 38275-57-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 38275-57-9 ]

CAS No. :38275-57-9 MDL No. :MFCD02940446
Formula : C5H2BrN3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VPQICCOHFSGBMA-UHFFFAOYSA-N
M.W : 183.99 Pubchem ID :686546
Synonyms :

Calculated chemistry of [ 38275-57-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 34.45
TPSA : 49.57 ?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) : -6.75 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.49
Log Po/w (XLOGP3) : 0.95
Log Po/w (WLOGP) : 1.11
Log Po/w (MLOGP) : -0.25
Log Po/w (SILICOS-IT) : 1.58
Consensus Log Po/w : 0.97

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.07
Solubility : 1.56 mg/ml ; 0.00846 mol/l
Class : Soluble
Log S (Ali) : -1.58
Solubility : 4.86 mg/ml ; 0.0264 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.59
Solubility : 0.472 mg/ml ; 0.00256 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.79

Safety of [ 38275-57-9 ]

Signal Word:Danger Class:9
Precautionary Statements:P273-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P305+P351+P338+P310 UN#:3077
Hazard Statements:H302+H312+H332-H315-H318-H335-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 38275-57-9 ]

* 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 [ 38275-57-9 ]

[ 38275-57-9 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 75-16-1 ]
  • [ 38275-57-9 ]
  • [ 1189169-37-6 ]
YieldReaction ConditionsOperation in experiment
61% at -78℃; for 3.5 h; 1-(5-Bromopyrimidin-2-yl)ethanone
To a solution of 5-bromopyrimidine-2-carbonitrile (221 mg, 1.2 mmol) in THF (10 ml) was added methylmagnesium bromide (3.0 ml, 4.20 mmol, 1.4 molar, THF) at -78° C. under nitrogen.
The solution was stirred at -78° C. for 3.5 hours, and then quenched with satd aq NH4Cl, and extracted with EtOAc.
The combined organic layer was dried over anhydrous Na2SO4 and concentrated.
The reaction was purified by column chromatography on silica gel (petroleum ether: EtOAc=1:0 to 0:1) to afford 1-(5-bromopyrimidin-2-yl)ethanone (1.55 mg, 61percent yield).
1H NMR (CDCl3 500 MHz): δ 9.00 (s, 2H), 2.80 (s, 3H).
Reference: [1] Patent: US2014/107335, 2014, A1, . Location in patent: Paragraph 0172; 0173
[2] Patent: WO2018/97945, 2018, A1, . Location in patent: Paragraph 0528
[3] Patent: US2009/253708, 2009, A1, . Location in patent: Page/Page column 15
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