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[ CAS No. 6914-79-0 ] {[proInfo.proName]}

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Inaccessible (Haz class 6.1), International USD 150+
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Chemical Structure| 6914-79-0
Chemical Structure| 6914-79-0
Structure of 6914-79-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6914-79-0 ]

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Product Details of [ 6914-79-0 ]

CAS No. :6914-79-0 MDL No. :MFCD00190651
Formula : C5H5NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :KSJJMSKNZVXAND-UHFFFAOYSA-N
M.W : 111.10 Pubchem ID :2733259
Synonyms :

Calculated chemistry of [ 6914-79-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.6
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 25.3
TPSA : 61.09 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.96 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.72
Log Po/w (XLOGP3) : 0.02
Log Po/w (WLOGP) : 0.31
Log Po/w (MLOGP) : -0.48
Log Po/w (SILICOS-IT) : 0.41
Consensus Log Po/w : 0.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.48
Solubility : 37.2 mg/ml ; 0.335 mol/l
Class : Very soluble
Log S (Ali) : -0.85
Solubility : 15.5 mg/ml ; 0.14 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.1
Solubility : 88.9 mg/ml ; 0.8 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.2

Safety of [ 6914-79-0 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H302+H312+H332-H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 6914-79-0 ]

* 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 [ 6914-79-0 ]

[ 6914-79-0 ] Synthesis Path-Downstream   1~13

  • 2
  • [ 6914-79-0 ]
  • [ 598-10-7 ]
  • 3
  • [ 6914-79-0 ]
  • [ 88157-18-0 ]
  • 4
  • [ 6914-79-0 ]
  • [ 100-51-6 ]
  • [ 148332-48-3 ]
  • 5
  • [ 67-56-1 ]
  • [ 6914-79-0 ]
  • [ 6914-73-4 ]
  • 6
  • [ 6914-79-0 ]
  • [ 139126-45-7 ]
  • 7
  • [ 6914-79-0 ]
  • aqueous KOH-solution [ No CAS ]
  • [ 598-10-7 ]
  • 9
  • [ 6914-79-0 ]
  • 1-trifluoromethyl-cyclopropanecarbonitrile [ No CAS ]
  • 10
  • [ 123-75-1 ]
  • [ 6914-79-0 ]
  • 1-[(1-cyanocyclopropyl)carbonyl]pyrrolidine [ No CAS ]
  • 11
  • [ 110-89-4 ]
  • [ 6914-79-0 ]
  • [ 546114-01-6 ]
  • 12
  • [ 110-91-8 ]
  • [ 6914-79-0 ]
  • 1-[(1-cyanocyclopropyl)carbonyl]morpholine [ No CAS ]
  • 13
  • [ 6914-79-0 ]
  • [ 139126-42-4 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In toluene; at 80℃; for 0.25h; The compound was prepared according to the procedure for Intermediate 3, starting from Intermediate 2 and 1-cyanocyclopropanecarbonyl chloride (generated in situ from 1- cyanocyclopropanecarboxylic acid and excess thionyl chloride in toluene at 800C for 15 min.). APCI-MS m/z: 576 [MH+].
With oxalyl dichloride;N,N-dimethyl-formamide; In dichloromethane; Compound 1-238[00461] To a solution of l-cyanocyclopropanecarboxylic acid (10 equiv) in dichloromethane was added oxalyl chloride (9 equiv) and catalytic N,iV-dimethylformamide. Once gas evolution ceased, this crude reaction mixture was added portion- wise to a suspension of Compound 1-107 (1 equiv) in dichloromethane/pyridine (1 :1) until complete consumption of starting material was observed by LS/MS. Purification via washing residual solid with diethyl ether following an aqueous ammonium chloride and dichloromethane workup (and subsequent concentration of organics) provided the desired compound as a yellow solid (27percent).1H NMR (400 MHz, DMSO-i/6) 9.41 (s, IH), 9.09 (d, IH), 8.04 (s, IH), 7.53 (s, IH), 7.41- 7.30 (m, IH), 7.24 (d, IH), 7.24-7.20 (m, IH), 7.11 (t, IH), 7.03 (bs, IH), 6.86 (t, IH), 5.90 (s, 2H), 1.72-1.64 (m, 4H) ppm.
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; at 0℃; for 2h; [00248] To a solution of 1-cyanocyclopropanecarboxylic acid (80 mg, 0.72 mmol) and oxalyl dichloride (136 mg, 1.08 mmol) in DCM (5 mL) was added a drop of DMF at 0 °C, then the mixture was stirred for 2 h, after completion the reaction mixture solution was used for next step directly.
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