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[ CAS No. 1885-38-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1885-38-7
Chemical Structure| 1885-38-7
Structure of 1885-38-7 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1885-38-7 ]

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Product Details of [ 1885-38-7 ]

CAS No. :1885-38-7 MDL No. :MFCD00001930
Formula : C9H7N Boiling Point : No data available
Linear Structure Formula :- InChI Key :ZWKNLRXFUTWSOY-QPJJXVBHSA-N
M.W : 129.16 Pubchem ID :1550846
Synonyms :

Calculated chemistry of [ 1885-38-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 41.09
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) : -5.7 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.82
Log Po/w (XLOGP3) : 1.96
Log Po/w (WLOGP) : 2.11
Log Po/w (MLOGP) : 2.01
Log Po/w (SILICOS-IT) : 2.3
Consensus Log Po/w : 2.04

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.25
Solubility : 0.72 mg/ml ; 0.00558 mol/l
Class : Soluble
Log S (Ali) : -2.08
Solubility : 1.06 mg/ml ; 0.00823 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.53
Solubility : 0.378 mg/ml ; 0.00292 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.99

Safety of [ 1885-38-7 ]

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

Application In Synthesis of [ 1885-38-7 ]

* 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 [ 1885-38-7 ]

[ 1885-38-7 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 1885-38-7 ]
  • [ 2286-54-6 ]
  • 2
  • [ 1885-38-7 ]
  • [ 326-62-5 ]
  • 2-(2-fluorophenyl)-3-phenylglutaronitrile [ No CAS ]
  • 3
  • [ 7446-70-0 ]
  • [ 1885-38-7 ]
  • [ 71-43-2 ]
  • [ 2286-54-6 ]
  • 4
  • [ 1885-38-7 ]
  • [ 98-80-6 ]
  • [ 2286-54-6 ]
  • 5
  • [ 1885-38-7 ]
  • [ 538-28-3 ]
  • 3-phenyl-3-benzylthiopropanenitrile [ No CAS ]
  • 6
  • [ 1885-38-7 ]
  • [ 2996-92-1 ]
  • [ 2286-54-6 ]
  • 7
  • [ 853955-69-8 ]
  • [ 1885-38-7 ]
  • [ 2286-54-6 ]
  • 8
  • [ 591-50-4 ]
  • [ 64-17-5 ]
  • [ 107-13-1 ]
  • [ 1885-38-7 ]
  • [ 3531-24-6 ]
  • [ 2286-54-6 ]
  • [ 645-59-0 ]
  • [ 2141-62-0 ]
  • 9
  • [ 1885-38-7 ]
  • [ 60100-09-6 ]
  • [ 23069-99-0 ]
  • [ 93948-20-0 ]
YieldReaction ConditionsOperation in experiment
46%Spectr.; 39%Spectr. With nickel; hydrogen; In tert-butyl alcohol; at 70℃; under 760.051 Torr; for 16h; General procedure: To a suspension of 0.4 g (0.012 mol) of sodium borohydride in 20 mL of piperidine 6a at 30C was added 0.8 g (0.006 mol) of anhydrous nickel(II) chloride. The mixture was heated to 60C to produce black colloid solution of a catalyst. Butyronitrile (6.9 g, 0.1 mol) was added to the resulting catalyst, and hydrogen was passed at 70C for 14 h. After cooling, 1 mL of water was added to the mixture to accelerate the catalyst coagulation. The precipitate was filtered off, the filtrate was analyzed. N-n-Butylidene-n-butylamine (5a), content 8%. Mass spectrum, m/e (Irel, %): 128.8 (13) [M + 2], 127.8 (100) [M + 1], 125.9 (4), 111.9 (16), 85.1 (8), 84.1 (53), 83.2 (9), 70.2 (16), 57.2 (26), 56.2 (30), 55.2 (10), 42.1 (50), 41.2 (34), 40.2 (3). N-n-Butylpiperidin (7a), content 19%. Mass spectrum, m/e (Irel,%): 141.9 (6) [M + 1], 140.7 (2) [M], 139.9 (5), 98.9 (6), 98.0 (100), 70.0 (10), 42.1 (7). N-1-Butyl-1-idenpiperidin (8a), content 39%. Mass spectrum, m/e (Irel, %): 139.9 (4) [M + 1], 138.8 (20) [M], 138.0 (7), 125.0 (9), 124.0 (100), 110.0 (8), 96.0 (4), 94.0 (5), 68.0 (20), 42.2 (6), 41.2 (9). N-1-Butyl-1-idendi-nbutylamine (9), content 31%. Mass spectrum, m/e (Irel, %): 183.0 (12) [M], 182.0 (100), 181.1 (9), 152.2 (6), 124.0 (5), 41.2 (3).
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