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[ CAS No. 10602-00-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 10602-00-3
Chemical Structure| 10602-00-3
Structure of 10602-00-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 10602-00-3 ]

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Product Details of [ 10602-00-3 ]

CAS No. :10602-00-3 MDL No. :MFCD00168819
Formula : C9H6O2 Boiling Point : -
Linear Structure Formula :HCCC6H4C(O)OH InChI Key :SJXHLZCPDZPBPW-UHFFFAOYSA-N
M.W : 146.14 Pubchem ID :589706
Synonyms :

Calculated chemistry of [ 10602-00-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 41.34
TPSA : 37.3 ?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) : -5.66 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.63
Log Po/w (XLOGP3) : 2.15
Log Po/w (WLOGP) : 1.45
Log Po/w (MLOGP) : 2.16
Log Po/w (SILICOS-IT) : 1.84
Consensus Log Po/w : 1.85

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.44
Solubility : 0.533 mg/ml ; 0.00365 mol/l
Class : Soluble
Log S (Ali) : -2.57
Solubility : 0.397 mg/ml ; 0.00272 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.83
Solubility : 2.15 mg/ml ; 0.0147 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.48

Safety of [ 10602-00-3 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 10602-00-3 ]

* 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.

  • Downstream synthetic route of [ 10602-00-3 ]

[ 10602-00-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 111291-97-5 ]
  • [ 10602-00-3 ]
  • 2
  • [ 619-58-9 ]
  • [ 10602-00-3 ]
  • [ 16819-43-5 ]
  • [ 116075-75-3 ]
  • 3
  • [ 925692-74-6 ]
  • [ 10602-00-3 ]
  • [ 124480-95-1 ]
  • 3-[4-(3,5-diethoxybenzoyloxy)phenyl]-5-(4-cyanophenyl)-isoxazole [ No CAS ]
  • 4
  • [ 16450-41-2 ]
  • [ 10602-00-3 ]
  • [ 111291-97-5 ]
  • [ 51766-21-3 ]
  • [ 116387-23-6 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; methanol; dichloromethane; EXAMPLE 7 Diethyl N-(4-ethynylbenzoyl)-L-glutamate To a solution of 0.55 g of 4-ethynylbenzoic acid (obtained from <strong>[111291-97-5]tert.-butyl 4-ethynylbenzoate</strong> in 84% yield by hydrolysis with trifluoroacetic acid) in 50 ml of anhydrous ether and 25 ml of anhydrous tetrahydrofuran is added 1.58 ml of triethylamine. This is followed by 1.00 g of phenyl N-phenylphosphoramidochloridate. After stirring the reaction mixture at room temperature under nitrogen for 0.5 hour, 0.90 g of diethyl L-glutamate is added in one portion. The mixture is allowed to stir for another 8 hrs. After a workup, the residue is subjected to column chromatography using a 1% methanol:methylene chloride mixture as the eluent. The major fraction isolated from the column contained 0.68 g (54%) of diethyl N-(ethynylbenzoyl)-L-glutamate as an oil which slowly solidified: NMR (CDCl3, 300 MHz) delta 1.25 (t, 3H, J=6.9 Hz), 1.33 (t, 3H, J=6.9 Hz), 2.11-2.60 (m, 4H), 3.23 (s, 1H), 4.09 (q, 2H, J=6.9 Hz), 4.27 (1, 2H, J=6.9 Hz), 4.80 (m, 1H), 7.12 (d, 1H, J=7.2 Hz), 7.59 (d, 2H, J=8.4 Hz), 7.81 (d, 2H, J=8.4 Hz); IR (KBr) 3330, 3280, 2990, 1735, 1640, 1520, 1380, 1200, 1105, 1020, 855, and 770 cm -1.
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