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[ CAS No. 127946-77-4 ] {[proInfo.proName]}

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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 127946-77-4
Chemical Structure| 127946-77-4
Structure of 127946-77-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 127946-77-4 ]

CAS No. :127946-77-4 MDL No. :MFCD04114063
Formula : C4H7ClN2 Boiling Point : -
Linear Structure Formula :- InChI Key :PCEIEQLJYDMRFZ-UHFFFAOYSA-N
M.W : 118.57 Pubchem ID :14586363
Synonyms :

Calculated chemistry of [ 127946-77-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 28.69
TPSA : 49.81 ?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 : Yes
Log Kp (skin permeation) : -6.87 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 0.22
Log Po/w (WLOGP) : 0.74
Log Po/w (MLOGP) : -0.31
Log Po/w (SILICOS-IT) : 0.33
Consensus Log Po/w : 0.2

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.71
Solubility : 22.9 mg/ml ; 0.193 mol/l
Class : Very soluble
Log S (Ali) : -0.83
Solubility : 17.7 mg/ml ; 0.149 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.31
Solubility : 57.9 mg/ml ; 0.489 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.47

Safety of [ 127946-77-4 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P280-P301+P310-P305+P351+P338 UN#:3439
Hazard Statements:H301-H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 127946-77-4 ]

* 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 [ 127946-77-4 ]

[ 127946-77-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 85-42-7 ]
  • [ 114041-16-6 ]
  • [ 127946-77-4 ]
  • [ 1403499-41-1 ]
  • 2
  • [ 187669-60-9 ]
  • [ 85-42-7 ]
  • [ 127946-77-4 ]
  • [ 1095534-28-3 ]
  • 3
  • [ 97914-59-5 ]
  • [ 127946-77-4 ]
  • N-(1-cyanocyclopropyl)-2-(difluoromethoxy)benzamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
42% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In N,N-dimethyl-formamide; at 0 - 20℃; for 12h; To a stirred solution of 2-(difluoro methoxy)benzoic acid (1g, 5.32 mmol) and 1- aminocyclopropane-1-carbonitrile hydrochloride (747 mg, 6.40 mmol) in DMF (20 mL) at 0oC were added TEA (3.0 mL, 21.28 mmol), EDC.HCl (1.52 mg, 7.98 mmol) and HOBt (1.07 mg, 7.98 mmol). Then the resulting reaction mixture was stirred at room temperature for 12h. After the completion of reaction, the mixture was diluted with ice cold water and extracted with EtOAc. The combined organic layers was washed with ice cold water (3 x 100 mL), brine (2 x 100mL) and dried over Na2SO4. Concentration followed by the purification of the crude product using flash column chromatography to afford N-(1- cyanocyclopropyl)-2-(difluoro methoxy)benzamide (560 mg, yield: 42 %) as an off-white solid.1H NMR (400 MHz, DMSO): δ 9.20 (s, 1H), 7.51-7.56 (m, 2H), 6.94-7.34 (m, 3H), 1.53-1.57 (m, 2H), 1.18-1.22(m, 2H). LC-MS (ESI): m/z 400.1 (M+H) +
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