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[ CAS No. 787-70-2 ] {[proInfo.proName]}

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Chemical Structure| 787-70-2
Chemical Structure| 787-70-2
Structure of 787-70-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 787-70-2 ]

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Product Details of [ 787-70-2 ]

CAS No. :787-70-2 MDL No. :MFCD00002554
Formula : C14H10O4 Boiling Point : -
Linear Structure Formula :HCOOC6H4C6H4COOH InChI Key :NEQFBGHQPUXOFH-UHFFFAOYSA-N
M.W : 242.23 Pubchem ID :13084
Synonyms :
4,4'-Bibenzoic acid
Chemical Name :[1,1'-Biphenyl]-4,4'-dicarboxylic acid

Calculated chemistry of [ 787-70-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 65.8
TPSA : 74.6 Ų

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 : No
Log Kp (skin permeation) : -5.45 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.53
Log Po/w (XLOGP3) : 3.28
Log Po/w (WLOGP) : 2.75
Log Po/w (MLOGP) : 2.68
Log Po/w (SILICOS-IT) : 2.3
Consensus Log Po/w : 2.51

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.7
Solubility : 0.0479 mg/ml ; 0.000198 mol/l
Class : Soluble
Log S (Ali) : -4.52
Solubility : 0.00729 mg/ml ; 0.0000301 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -3.67
Solubility : 0.052 mg/ml ; 0.000215 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 787-70-2 ]

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

Application In Synthesis of [ 787-70-2 ]

* 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 [ 787-70-2 ]

[ 787-70-2 ] Synthesis Path-Downstream   1~9

  • 2
  • [ 5743-04-4 ]
  • [ 787-70-2 ]
  • [ 91296-87-6 ]
  • [Cd2(sarafloxacin)2(4,4'-biphenyldicarboxylato)2]*4.5H2O [ No CAS ]
  • 3
  • [ 4054-67-5 ]
  • [ 6147-53-1 ]
  • [ 787-70-2 ]
  • [ 68-12-2 ]
  • [ 75-05-8 ]
  • [Co2(4,4′-biphenyldicarboxylate)1.5(3,3′,5,5′-tetramethyl-4,4′-bipyrazole(1-))]·DMF·CH3CN·H2O [ No CAS ]
  • 4
  • [ 4054-67-5 ]
  • [ 6147-53-1 ]
  • [ 787-70-2 ]
  • [ 68-12-2 ]
  • [Co2(4,4′-biphenyldicarboxylicacid)2(3,3′,5,5′-tetramethyl-4,4′-bipyrazole)]*2(DMF)*5(H2O) [ No CAS ]
YieldReaction ConditionsOperation in experiment
23.4% In acetonitrile; at 140℃; for 72.0h; A mixture of Co(CH3COO)2·4H2O (0.050 g, 0.20 mmol), H2bpdc (0.072 g, 0.30 mmol) and H2bpz (0.038 g, 0.20 mmol) in DMF (5 mL) and CH3CN (5 mL) was placed in a Teflon-lined stainless steel vessel (15 mL). The vessel was heated at 140 C for 72 h, then slowly cooled to room temperature. The purple crystals of 1 were isolated by filtrating, washing with DMF, and dried in vacuo. Yield: 24 mg (23.4%). Anal. Calcd for C44H54Co2N6O15: C, 51.57; H, 5.31; N, 8.20%. Found: C, 51.45; H, 5.17; N, 8.11%. IR (KBr, cm-1): 3426(vs), 2919(w), 1680(s), 1605(s), 1540(m), 1394(s), 1297(m), 1172(w), 1130(w), 851(m), 765(s).
  • 5
  • zinc(II) sulfate heptahydrate [ No CAS ]
  • [ 4054-67-5 ]
  • [ 787-70-2 ]
  • [Zn4(3,3′,5,5′-tetramethyl-4,4′-bipyrazole)2(biphenyl-4,4′-dicarboxylic acid)3]n [ No CAS ]
  • 6
  • europium(III) chloride hexahydrate [ No CAS ]
  • [ 865169-07-9 ]
  • [ 787-70-2 ]
  • Eu(3+)*C20H11N4O2(1-)*C14H8O4(2-) [ No CAS ]
  • 7
  • [ 10196-18-6 ]
  • [ 4054-67-5 ]
  • [ 787-70-2 ]
  • [Zn4O(3,3',5,5'-tetramethyl-4,4'-bipyrazole)2(biphenyl-4,4'-dicarboxylic acid)] [ No CAS ]
  • 8
  • [ 792-74-5 ]
  • [ 787-70-2 ]
YieldReaction ConditionsOperation in experiment
96.6% With sulfuric acid; In water; acetic acid; at 120℃; for 24h;Reflux; The detailed procedure is as follows; to the solution of MBPDC (600 mg, 2.22 mmol) in 40 mL acetic acid, 20 mL of4:1 (v/v) H2SO4/H2O solution was added. Then the reaction mixture was refluxed for 24 h at 120C. The product was washed thoroughl ywith ethanol and dried in oven at 80°C overnight (Yield: 520 mg,96.6percent).
  • 9
  • [ 787-70-2 ]
  • [ 1791-13-5 ]
  • tetra-tert-butyl 2,2'-(([1,1'-biphenyl]-4,4'-dicarbonyl)bis(azanediyl))(2S,2'S)-disuccinate [ No CAS ]
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