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[ CAS No. 207557-35-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 207557-35-5
Chemical Structure| 207557-35-5
Structure of 207557-35-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 207557-35-5 ]

CAS No. :207557-35-5 MDL No. :MFCD08689902
Formula : C7H9ClN2O Boiling Point : -
Linear Structure Formula :- InChI Key :YCWRPKBYQZOLCD-LURJTMIESA-N
M.W : 172.61 Pubchem ID :11073883
Synonyms :

Calculated chemistry of [ 207557-35-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.71
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.2
TPSA : 44.1 ?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) : -6.89 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.26
Log Po/w (XLOGP3) : 0.65
Log Po/w (WLOGP) : 0.36
Log Po/w (MLOGP) : 0.17
Log Po/w (SILICOS-IT) : 1.0
Consensus Log Po/w : 0.69

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.19
Solubility : 11.2 mg/ml ; 0.0649 mol/l
Class : Very soluble
Log S (Ali) : -1.15
Solubility : 12.2 mg/ml ; 0.0705 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.15
Solubility : 12.3 mg/ml ; 0.0714 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.0

Safety of [ 207557-35-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P501-P261-P270-P271-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330-P304+P340+P312-P403+P233-P405 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 207557-35-5 ]

* 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.

  • Downstream synthetic route of [ 207557-35-5 ]

[ 207557-35-5 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 137583-05-2 ]
  • [ 207557-35-5 ]
  • 1[-2-[(pyrimidin-2-yl)amino]ethylamino]acetyl-2-cyano-(S)-pyrrolidine [ No CAS ]
  • 2
  • [ 45887-08-9 ]
  • [ 207557-35-5 ]
  • (2S)-1-[1,1-Dimethyl-3-(3-pyridin-3-yl-pyrazol-1-yl)-propylamino]-acetyl}-pyrrolidine-2-carbonitrile, methanesulfonic acid salt [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 97 (2S)-1-[1,1-Dimethyl-3-(3-pyridin-3-yl-pyrazol-1-yl)-propylamino]-acetyl}-pyrrolidine-2-carbonitrile, Methanesulfonic Acid Salt This compound was made in analogy to example 78, steps C] to D] from 3-(1H-pyrazol-3-yl)-pyridine (synthesised according to the literature: Plate et al., Bioorg. Med. Chem. 1996, 4 (2), 227 and Schunack, Arch. Pharm. 1973, 306, 934, 941), 4,4-dimethyl-2,2-dioxo-2λ'-[1,2,3]oxathiazinane-3-carboxylic acid tert-butyl ester and IIA as a methanesulfonic acid addition salt. MS (ISP): 367.3 (MH+, free base).
  • 3
  • sulfimidate [ No CAS ]
  • [ 3347-62-4 ]
  • [ 207557-35-5 ]
  • (2S)-1-[(1S)-1-Methyl-2-(5-methyl-3-phenyl-pyrazol-1-yl)-ethylamino]-acetyl}-pyrrolidine-2-carbonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
Example 112 (2S)-1-[(1S)-1-Methyl-2-(5-methyl-3-phenyl-pyrazol-1-yl)-ethylamino]-acetyl}-pyrrolidine-2-carbonitrile The title compound was obtained in analogy to example 78, steps C] to E] from <strong>[3347-62-4]5-methyl-3-phenyl-1H-pyrazole</strong> by replacing sulfimidate XIX with IV and with the exception, that the final coupling step with IIA was done as described in example 1. The title compound was obtained as the free amine as a glass. MS (ISP): 352.4 (MH+).
  • 4
  • [ 228244-04-0 ]
  • [ 207557-35-5 ]
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