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[ CAS No. 1846598-27-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1846598-27-3
Chemical Structure| 1846598-27-3
Structure of 1846598-27-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1846598-27-3 ]

CAS No. :1846598-27-3 MDL No. :MFCD32856534
Formula : C56H40N6 Boiling Point : -
Linear Structure Formula :- InChI Key :ZOMQCVKHGOMNER-UHFFFAOYSA-N
M.W : 796.96 Pubchem ID :146162400
Synonyms :

Calculated chemistry of [ 1846598-27-3 ]

Physicochemical Properties

Num. heavy atoms : 62
Num. arom. heavy atoms : 54
Fraction Csp3 : 0.0
Num. rotatable bonds : 12
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 254.6
TPSA : 60.54 Ų

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -1.0 cm/s

Lipophilicity

Log Po/w (iLOGP) : 5.51
Log Po/w (XLOGP3) : 14.31
Log Po/w (WLOGP) : 15.31
Log Po/w (MLOGP) : 8.58
Log Po/w (SILICOS-IT) : 9.0
Consensus Log Po/w : 10.54

Druglikeness

Lipinski : 2.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 3.0
Bioavailability Score : 0.17

Water Solubility

Log S (ESOL) : -13.65
Solubility : 0.0 mg/ml ; 0.0 mol/l
Class : Insoluble
Log S (Ali) : -15.67
Solubility : 0.0 mg/ml ; 2.13e-16 mol/l
Class : Insoluble
Log S (SILICOS-IT) : -19.45
Solubility : 2.8e-17 mg/ml ; 3.51e-20 mol/l
Class : Insoluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 3.0
Synthetic accessibility : 5.56

Safety of [ 1846598-27-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1846598-27-3 ]

* 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 [ 1846598-27-3 ]

[ 1846598-27-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 122-39-4 ]
  • [ 2377-81-3 ]
  • [ 1846598-27-3 ]
YieldReaction ConditionsOperation in experiment
90% Stage #1: diphenylamine With sodium hydride In tetrahydrofuran at 20℃; for 0.75h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran at 20℃; for 12h; Inert atmosphere;
86% Stage #1: diphenylamine With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran at 20℃; for 12h; Inert atmosphere;
66% Stage #1: diphenylamine With sodium hydride In tetrahydrofuran at 60℃; for 1h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran at 40℃; Inert atmosphere;
62% Stage #1: diphenylamine With sodium hydride In tetrahydrofuran at 60℃; for 1h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran at 40 - 60℃; Inert atmosphere;
62% Stage #1: diphenylamine With sodium hydride In N,N-dimethyl-formamide at 60℃; for 0.5h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile at 20 - 40℃; for 24h;
50% Stage #1: diphenylamine With sodium hydride In N,N-dimethyl-formamide; mineral oil at 20℃; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In N,N-dimethyl-formamide; mineral oil at 20℃; for 15h; Inert atmosphere;
Stage #1: diphenylamine With sodium hydride In tetrahydrofuran at 20℃; for 0.75h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran at 20℃; for 12h; Inert atmosphere;
Stage #1: diphenylamine With sodium hydride In tetrahydrofuran; mineral oil at 20℃; for 0.5h; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran; mineral oil at 20℃; for 12h;
With sodium hydride In N,N-dimethyl-formamide at 50℃; for 5h; Inert atmosphere;
Stage #1: diphenylamine With sodium hydride In tetrahydrofuran; mineral oil Cooling with ice; Inert atmosphere; Schlenk technique; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran; mineral oil Cooling with ice; Inert atmosphere;
62 % Stage #1: diphenylamine With sodium hydride In tetrahydrofuran; mineral oil at 60℃; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In tetrahydrofuran; mineral oil Inert atmosphere; Heating;
62 % Stage #1: diphenylamine With sodium hydride In N,N-dimethyl-formamide; mineral oil at 60℃; Inert atmosphere; Stage #2: tetrafluoroisophthalonitrile In N,N-dimethyl-formamide; mineral oil at 20 - 40℃; Inert atmosphere;

Reference: [1]Shee, Maniklal; Shah, Sk. Sheriff; Singh, N. D. Pradeep [Chemistry - A European Journal, 2020, vol. 26, # 62, p. 14070 - 14074]
[2]Li, Weiyu; Chen, Xiaofei; Zhou, Lei [Organic Letters, 2022, vol. 24, # 32, p. 5946 - 5950]
[3]Chernowsky, Colleen P.; Chmiel, Alyah F.; Wickens, Zachary K. [Angewandte Chemie - International Edition, 2021, vol. 60, # 39, p. 21418 - 21425][Angew. Chem., 2021, vol. 133, # 39, p. 21588 - 21595]
[4]Chernowsky, Colleen P.; Chmiel, Alyah F.; Wickens, Zachary K.; Williams, Oliver P.; Yeung, Charles S. [Journal of the American Chemical Society, 2021, vol. 143, # 29, p. 10882 - 10889]
[5]Alektiar, Sara N.; Wickens, Zachary K. [Journal of the American Chemical Society, 2021, vol. 143, # 33, p. 13022 - 13028]
[6]Garreau, Marion; Le Vaillant, Franck; Waser, Jerome [Angewandte Chemie - International Edition, 2019, vol. 58, # 24, p. 8182 - 8186][Angew. Chem., 2019, vol. 131, p. 8266 - 8270,5]
[7]Shah, Sk. Sheriff; Shee, Maniklal; Singh, N. D. Pradeep [Chemical Communications, 2020, vol. 56, # 30, p. 4240 - 4243]
[8]Liu, Yan; Chen, Xiao-Lan; Li, Xiao-Yun; Zhu, Shan-Shan; Li, Shi-Jun; Song, Yan; Qu, Ling-Bo; Yu, Bing [Journal of the American Chemical Society, 2021, vol. 143, # 2, p. 964 - 972]
[9]Zhou, Chao; Gan, Qi-Chao; Zhou, Tai-Ping; Lei, Tao; Ye, Chen; He, Xiao-Jun; Chen, Bin; Lu, Heng; Wan, Qian; Liao, Rong-Zhen; Tung, Chen-Ho; Wu, Li-Zhu [Angewandte Chemie - International Edition, 2022, vol. 61, # 10][Angew. Chem., 2022, vol. 134, # 10]
[10]Zeng, Liang; Qin, Jing-Hao; Lv, Gui-Fen; Hu, Ming; Sun, Qing; Ouyang, Xuan-Hui; He, De-Liang; Li, Jin-Heng [Chinese Journal of Chemistry, 2023, vol. 41, # 16, p. 1921 - 1930]
[11]Williams, Oliver P.; Chmiel, Alyah F.; Mikhael, Myriam; Bates, Desiree M.; Yeung, Charles S.; Wickens, Zachary K. [Angewandte Chemie - International Edition, 2023, vol. 62, # 18][Angew. Chem., 2023, vol. 135, # 18]
[12]Alektiar, Sara N.; Han, Jimin; Dang; Rubel, Camille Z.; Wickens, Zachary K. [Journal of the American Chemical Society, 2023, vol. 145, # 20, p. 10991 - 10997]
  • 2
  • [ 626-17-5 ]
  • [ 122-39-4 ]
  • [ 1846598-27-3 ]
YieldReaction ConditionsOperation in experiment
76 % Stage #1: diphenylamine With sodium hydride In dimethyl sulfoxide Schlenk technique; Inert atmosphere; Stage #2: benzene-1,3-dicarbonitrile In dimethyl sulfoxide at 20℃; Schlenk technique; Inert atmosphere;
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