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[ CAS No. 606-45-1 ] {[proInfo.proName]}

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Chemical Structure| 606-45-1
Chemical Structure| 606-45-1
Structure of 606-45-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 606-45-1 ]

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Product Details of [ 606-45-1 ]

CAS No. :606-45-1 MDL No. :MFCD00008423
Formula : C9H10O3 Boiling Point : -
Linear Structure Formula :- InChI Key :PFYHAAAQPNMZHO-UHFFFAOYSA-N
M.W : 166.17 Pubchem ID :61151
Synonyms :

Calculated chemistry of [ 606-45-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.21
TPSA : 35.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.13
Log Po/w (XLOGP3) : 2.04
Log Po/w (WLOGP) : 1.48
Log Po/w (MLOGP) : 1.64
Log Po/w (SILICOS-IT) : 1.7
Consensus Log Po/w : 1.8

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.33
Solubility : 0.782 mg/ml ; 0.0047 mol/l
Class : Soluble
Log S (Ali) : -2.41
Solubility : 0.64 mg/ml ; 0.00385 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.59
Solubility : 0.424 mg/ml ; 0.00255 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.33

Safety of [ 606-45-1 ]

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

Applications of [ 606-45-1 ]

Methyl 2-methoxybenzoate (CAS: 606-45-1) can be used in the preparation of Salicylic acid (CAS: 69-72-7). Salicylic acid exhibits bacteriostatic, fungicidal, and keratolytic actions. Its salts, known as salicylates, are commonly used as analgesics.

Application In Synthesis of [ 606-45-1 ]

* 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 [ 606-45-1 ]

[ 606-45-1 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 606-45-1 ]
  • [ 5129-25-9 ]
  • [ 22802-67-1 ]
  • 2
  • [ 606-45-1 ]
  • [ 75-05-8 ]
  • [ 6609-56-9 ]
YieldReaction ConditionsOperation in experiment
66% With molybdenum hexacarbonyl; In tetrachloromethane; at 150℃; for 6h;Autoclave; General procedure: General procedure for the reaction of acetonitrilewith carboxylic acids. A 17-mL stainless-steelhigh-pressure microreactor was charged with 1 mmolof Mo(CO)6 or VO(acac)2, 100 mmol of carboxylicacid, 500 mmol of acetonitrile, and 50 mmol of carbontetrachloride. The reactor was hermetically closed andheated for 6 h at 150C. When the reaction wascomplete, the reactor was cooled to room temperatureand opened, the mixture was filtered through a layer ofAl2O3, unreacted acetonitrile and carbon tetrachloridewere distilled off, and the residue was distilled underatmospheric or reduced pressure or recrystallized fromethanol.
  • 3
  • [ 606-45-1 ]
  • [ 22802-67-1 ]
  • 4
  • [ 1493-13-6 ]
  • [ 606-45-1 ]
  • [ 1391728-13-4 ]
  • (2-(2-hydroxypropan-2-yl)phenyl)(4-methoxy-3-(methoxy carbonyl)-phenyl)iodonium triflate [ No CAS ]
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