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[ CAS No. 119-67-5 ] {[proInfo.proName]}

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Chemical Structure| 119-67-5
Chemical Structure| 119-67-5
Structure of 119-67-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 119-67-5 ]

CAS No. :119-67-5 MDL No. :MFCD00003336
Formula : C8H6O3 Boiling Point : -
Linear Structure Formula :(CHO)C6H4COOH InChI Key :DYNFCHNNOHNJFG-UHFFFAOYSA-N
M.W : 150.13 Pubchem ID :8406
Synonyms :

Calculated chemistry of [ 119-67-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 38.79
TPSA : 54.37 ?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) : -6.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.92
Log Po/w (XLOGP3) : 0.97
Log Po/w (WLOGP) : 1.2
Log Po/w (MLOGP) : 0.97
Log Po/w (SILICOS-IT) : 1.36
Consensus Log Po/w : 1.08

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.65
Solubility : 3.33 mg/ml ; 0.0222 mol/l
Class : Very soluble
Log S (Ali) : -1.7
Solubility : 3.0 mg/ml ; 0.02 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.7
Solubility : 2.99 mg/ml ; 0.0199 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 119-67-5 ]

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:

Application In Synthesis of [ 119-67-5 ]

* 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 [ 119-67-5 ]
  • Downstream synthetic route of [ 119-67-5 ]

[ 119-67-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 119-67-5 ]
  • [ 20361-09-5 ]
YieldReaction ConditionsOperation in experiment
34% With hydrogenchloride In methanol; water EXAMPLE 1
[1H]-Isoindolin-1-one-3-carboxylic acid
Ammonia gas was bubbled into a cooled (10°-15° C.) solution of 10 g (0.0666 mole) of phthalaldehydic acid in 100 ml of methanol for 10 minutes, and the solution allowed to stir at room temperature for one hour.
To the stirred solution was added a solution of 3.26 g (0.0666 mole) of sodium cyanide in 100 ml of water over a 15 minute period.
After stirring at room temperature for one hour, most of the methanol was removed in vacuo and the resulting yellow solution was treated dropwise with 80 ml of 6 N hydrochloric acid over a 10 minute period, producing a transient precipitate followed by redissolution.
The solution was heated at 100° C. for 1.5 hours, producing a thick yellow precipitate.
The mixture was cooled to room temperature, the yellow solid filtered and washed with water and acetone.
The resulting solid was recrystallized from water, 4.14 g (34percent yield), m.p. 153°-154° C.
The product displayed physical properties in complete agreement with those described in the literature, Darapsky, et al., J. Prakt. Chem., 146, 307 (1936).
Reference: [1] Patent: US4730056, 1988, A,
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