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[ CAS No. 3807-81-6 ] {[proInfo.proName]}

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Chemical Structure| 3807-81-6
Chemical Structure| 3807-81-6
Structure of 3807-81-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 3807-81-6 ]

CAS No. :3807-81-6 MDL No. :MFCD03839939
Formula : C9H5NO8 Boiling Point : No data available
Linear Structure Formula :- InChI Key :KIRNHRJGEAFKPM-UHFFFAOYSA-N
M.W : 255.14 Pubchem ID :14434859
Synonyms :

Calculated chemistry of [ 3807-81-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 4
Num. H-bond acceptors : 8.0
Num. H-bond donors : 3.0
Molar Refractivity : 56.14
TPSA : 157.72 ?2

Pharmacokinetics

GI absorption : Low
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) : -7.62 cm/s

Lipophilicity

Log Po/w (iLOGP) : -0.49
Log Po/w (XLOGP3) : 0.33
Log Po/w (WLOGP) : 0.69
Log Po/w (MLOGP) : -0.02
Log Po/w (SILICOS-IT) : -1.98
Consensus Log Po/w : -0.29

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 1.0
Egan : 1.0
Muegge : 1.0
Bioavailability Score : 0.11

Water Solubility

Log S (ESOL) : -1.61
Solubility : 6.23 mg/ml ; 0.0244 mol/l
Class : Very soluble
Log S (Ali) : -3.21
Solubility : 0.159 mg/ml ; 0.000623 mol/l
Class : Soluble
Log S (SILICOS-IT) : 0.1
Solubility : 318.0 mg/ml ; 1.25 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.14

Safety of [ 3807-81-6 ]

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 [ 3807-81-6 ]

* 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 [ 3807-81-6 ]

[ 3807-81-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 569-51-7 ]
  • [ 3807-81-6 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; potassium nitrate; In water; Petroleum ether; EXAMPLE 1 5-Nitro-<strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong> To a stirred mixture of 125 g. of <strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong> and 900 ml. of concentrated sulfuric acid at 60°-70° C. is added, gradually over a 2 hour period, 312 g. of potassium nitrate. The mixture is heated at 135°-140° C. for 16 hours, cooled and treated with ice and water. Some solid is seprated out and is dissolved in water. The entire aqueous mixture is extracted with ether, the extract is washed with water and dried over magnesium sulfate. The ether is concentrated to a small volume, and petroleum ether is added to precipitate a white solid. The solid is collected and dried to give 76.5 g. of the product of the Example.
With sulfuric acid; potassium nitrate; In water; Petroleum ether; EXAMPLE 9 5,5',5"-[1,3,6-Naphthalenetriyltris(sulfonylimino)]tri-<strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong> nonaphenyl ester To a stirred mixture of 125 g of <strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong> and 900 ml of concentrated sulfuric acid at 60°-70° C is added, gradually over a 2 hour period, 312 g of potassium nitrate. The mixture is heated at 135°-140° C for 16 hours, cooled and treated with ice and water. Some solid is separated out and is dissolved in water. The entire aqueous mixture is extracted with ether, the extract is washed with water and dried over magnesium sulfate. The ether is concentrated to a small volume, and petroleum ether is added to precipitate a white solid. The solid is collected and dried to give 76.5 g of 5-nitro-<strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong>.
With sulfuric acid; potassium nitrate; potassium hydroxide; In diethyl ether; water; isopropyl alcohol; The mass of raw materials <strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong>, potassium hydroxide, and isopropanol used for synthesizing intermediate are 5 g, 8.4 g, 275 g. Step (1) Synthesis of 5-nitro-<strong>[569-51-7]1,2,3-benzenetricarboxylic acid</strong> (B) The mass of the starting material of intermediate 1, concentrated sulfuric acid, potassium nitrate, ether, and deionized water used in the reaction product was 5.5 g, 55.9 g, 10.9 g, 228.3 g, 10 g, respectively.
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