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[ CAS No. 30515-28-7 ] {[proInfo.proName]}

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Chemical Structure| 30515-28-7
Chemical Structure| 30515-28-7
Structure of 30515-28-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 30515-28-7 ]

CAS No. :30515-28-7 MDL No. :MFCD00037800
Formula : C7H13BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :JLPQXFFMVVPIRW-UHFFFAOYSA-N
M.W : 209.08 Pubchem ID :121723
Synonyms :

Calculated chemistry of [ 30515-28-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 6
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 45.4
TPSA : 37.3 ?2

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) : -6.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 0.95
Log Po/w (WLOGP) : 2.42
Log Po/w (MLOGP) : 2.12
Log Po/w (SILICOS-IT) : 1.99
Consensus Log Po/w : 1.88

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.34
Solubility : 9.58 mg/ml ; 0.0458 mol/l
Class : Very soluble
Log S (Ali) : -1.32
Solubility : 10.0 mg/ml ; 0.0478 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.54
Solubility : 0.602 mg/ml ; 0.00288 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.33

Safety of [ 30515-28-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 30515-28-7 ]

* 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 [ 30515-28-7 ]

[ 30515-28-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 30515-28-7 ]
  • [ 3575-32-4 ]
  • [ 1207983-32-1 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In ethanol; at 90℃; for 21h; Step 1 Preparation of 7-(3-Dimethylamino-phenviamino)-heptanoie acid [Int-4A1 Int-4A[0129] To a mixture of <strong>[3575-32-4]N,N-dimethyl-m-phenylenediamine dihydrochloride</strong> (663 mg, 3.17 mmol) and 7-bromoheptanoic acid (662 mg, 3.17 mmol) in 10 mL EtOH is added triethylamine (2.2 mL, 16 mmol). The reaction mixture becomes homogenous and is stirred at 90 C for 21 h. The reaction is cooled to room temperature and solvent is removed under reduced pressure. The crude product Int-4A is used directly in the following step. LC-MS m/z 265.2 (M+H), retention time 2.33 min.
  • 2
  • [ 30515-28-7 ]
  • [ 3575-32-4 ]
  • [ 1207983-31-0 ]
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