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[ CAS No. 628732-03-6 ] {[proInfo.proName]}

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Chemical Structure| 628732-03-6
Chemical Structure| 628732-03-6
Structure of 628732-03-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 628732-03-6 ]

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Product Details of [ 628732-03-6 ]

CAS No. :628732-03-6 MDL No. :MFCD11035916
Formula : C9H9NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :GZRHFGSCUQBJHR-UHFFFAOYSA-N
M.W : 147.17 Pubchem ID :12119264
Synonyms :

Calculated chemistry of [ 628732-03-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.89
TPSA : 43.09 ?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) : -6.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.4
Log Po/w (XLOGP3) : 1.54
Log Po/w (WLOGP) : 1.41
Log Po/w (MLOGP) : 1.05
Log Po/w (SILICOS-IT) : 2.04
Consensus Log Po/w : 1.49

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.13
Solubility : 1.1 mg/ml ; 0.00748 mol/l
Class : Soluble
Log S (Ali) : -2.05
Solubility : 1.3 mg/ml ; 0.00883 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.74
Solubility : 0.27 mg/ml ; 0.00184 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.42

Safety of [ 628732-03-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 628732-03-6 ]

* 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.

  • Downstream synthetic route of [ 628732-03-6 ]

[ 628732-03-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 32202-61-2 ]
  • [ 628732-03-6 ]
YieldReaction ConditionsOperation in experiment
Example SIXTEENbeta Procedure for the synthesis of 7-iodo-indan-1-one (Intermediate SIXTEENbeta3) "2 NHz o'0 v Method J S NaNO2, Kl S /z,, ---- y y Intermediate SIXTEENbeta 1 Intermediate Intermediate SIXTEENbeta3 SIXTEENbeta 2 Use of <strong>[32202-61-2]indan-4-ylamine</strong> (Intermediate SIXTEEN-beta-1) (commercially available from Aldrich) in Method J produced 7-amino-indan-1-one (Intermediate SIXTEENbeta-2). A mixture of [7-AMINO-INDAN-1-ONE] (Intermediate SIXTEENbeta-2) (1.44 g, 9.8 mmol) in water (11 mL), acetic acid (11 mL), and HCl (2.7 [ML)] was treated with a solution [OF NAN02] (0.75 g in 2.8 mL) at [0 C.] A solution of KI in water (1.76 g 10.4 mmol in 2.8 mL) was added and the mixture was heated to [60 C] for 1 h. The mixture was cooled and quenched with solid [NAHS03] followed by water. The product was extracted with CH2Cl2 (3x) and washed with sat. [NAHC03] and brine. The compound was purified by column chromatography on silica gel with 60 to 70% [CH2CL2] : hexane. [7-IODO-INDAN-L-ONE] (Intermediate SIXTEENbeta3) was isolated as a light yellow solid [(31%).]
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