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[ CAS No. 21423-81-4 ] {[proInfo.proName]}

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Chemical Structure| 21423-81-4
Chemical Structure| 21423-81-4
Structure of 21423-81-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 21423-81-4 ]

CAS No. :21423-81-4 MDL No. :MFCD00001799
Formula : C8H6ClN Boiling Point : -
Linear Structure Formula :- InChI Key :INEMHABDFCKBID-UHFFFAOYSA-N
M.W : 151.59 Pubchem ID :88894
Synonyms :

Calculated chemistry of [ 21423-81-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.13
TPSA : 23.79 ?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) : -4.86 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.01
Log Po/w (XLOGP3) : 3.33
Log Po/w (WLOGP) : 2.52
Log Po/w (MLOGP) : 2.37
Log Po/w (SILICOS-IT) : 2.9
Consensus Log Po/w : 2.63

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.32
Solubility : 0.0723 mg/ml ; 0.000477 mol/l
Class : Soluble
Log S (Ali) : -3.51
Solubility : 0.0472 mg/ml ; 0.000312 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.47
Solubility : 0.0515 mg/ml ; 0.00034 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.55

Safety of [ 21423-81-4 ]

Signal Word:Danger Class:4.1
Precautionary Statements:P210 UN#:1325
Hazard Statements:H228 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 21423-81-4 ]

* 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 [ 21423-81-4 ]

[ 21423-81-4 ] Synthesis Path-Downstream   1~6

  • 2
  • [ 21423-81-4 ]
  • [ 24377-95-5 ]
  • [ 117738-77-9 ]
  • 4
  • [ 21423-81-4 ]
  • [ 117738-77-9 ]
  • 2-chloro-terephthalamic acid [ No CAS ]
  • 5
  • [ 7664-93-9 ]
  • [ 21423-81-4 ]
  • dichromate [ No CAS ]
  • [ 24377-95-5 ]
  • [ 117738-77-9 ]
  • 2-chloro-terephthalamic acid [ No CAS ]
  • 6
  • [ 181074-22-6 ]
  • [ 21423-81-4 ]
  • [ 117738-77-9 ]
  • [ 529-34-0 ]
  • ethyl rac-(6-(N-(4-aminoiminomethyl-2-chlorobenzoyl)amino)-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetate hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine; thionyl chloride; In tetrahydrofuran; hexane; toluene; 5.7 g (31.4 mmol) of <strong>[117738-77-9]2-chloro-4-cyano-benzoic acid</strong>, which was prepared by oxidation of 3-chloro-4-methyl-benzonitrile (according to Chem. Ber. 1936, 69, 537, the disclosure of which is incorporated herein by reference), were dissolved in 300 ml toluene, and 10.25 g (86.2 mmol) thionyl chloride were added. After 4 hours heating with reflux the same amount of thionyl chloride was added and heating was continued overnight. The solvent was removed under reduced pressure, the residue dissolved in 100 ml toluene, and again it was concentrated in vacuo to leave the crude acid chloride as a yellow oil. Yield: 4.1 g (65%) A solution of 0.98 g (3.96 mmol) of the tetralone 98 and 3.3 ml dry pyridine in 33 ml dry THF was cooled with ice, and a solution of 1.0 g (5.0 mmol) of the crude 2-chloro-4-cyanobenzoyl chloride in 33 ml dry THF was added dropwise. The mixture was warmed slowly to room temperature, stirred over night, and poured into ice-cold water. The mixture was extracted with ethyl acetate, and the organic layer was washed with saturated aqueous sodium bicarbonate and with brine, successively, and dried over sodium sulfate. The product was concentrated under reduced pressure, and the residue was stirred with hexane to give the crystalline nitrile (280), which was filtered and dried in vacuo at 50 C. Yield: 1.5 g (92%) of beige crystalline solid, m.p. 173-175 C.
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