99.9%(GC)| A1453589|Formula:C5H8O4|Molecular Weight:132.114650000+ products instock " />

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[ CAS No. 110-94-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 110-94-1
Chemical Structure| 110-94-1
Structure of 110-94-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 110-94-1 ]

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Product Details of [ 110-94-1 ]

CAS No. :110-94-1 MDL No. :MFCD00004410
Formula : C5H8O4 Boiling Point : -
Linear Structure Formula :CO2H(CH2)3CO2H InChI Key :JFCQEDHGNNZCLN-UHFFFAOYSA-N
M.W : 132.11 Pubchem ID :743
Synonyms :
GA
Chemical Name :Glutaric acid

Calculated chemistry of [ 110-94-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.6
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 29.69
TPSA : 74.6 ?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) : -7.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.45
Log Po/w (XLOGP3) : -0.29
Log Po/w (WLOGP) : 0.33
Log Po/w (MLOGP) : -0.13
Log Po/w (SILICOS-IT) : -0.29
Consensus Log Po/w : 0.01

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -0.21
Solubility : 81.0 mg/ml ; 0.613 mol/l
Class : Very soluble
Log S (Ali) : -0.82
Solubility : 20.1 mg/ml ; 0.152 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.19
Solubility : 206.0 mg/ml ; 1.56 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.29

Safety of [ 110-94-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P280-P302+P352-P312-P337+P313-P305+P351+P338-P362+P364-P332+P313 UN#:N/A
Hazard Statements:H315-H319-H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 110-94-1 ]

* 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 [ 110-94-1 ]

[ 110-94-1 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 110-94-1 ]
  • [ 623-81-4 ]
  • [ 1070-62-8 ]
  • 2
  • [ 110-94-1 ]
  • [ 3452-97-9 ]
  • glutaric acid bis-(3,5,5-trimethyl-hexyl ester) [ No CAS ]
  • 3
  • [ 110-94-1 ]
  • [ 818-38-2 ]
  • [ 1070-62-8 ]
  • 4
  • [ 63128-51-8 ]
  • [ 110-94-1 ]
  • [ 115-11-7 ]
  • 5
  • [ 110-94-1 ]
  • [ 74-89-5 ]
  • [ 25077-25-2 ]
  • [ 56269-42-2 ]
  • 7
  • [ 110-94-1 ]
  • [ 1454-85-9 ]
  • [ 26720-17-2 ]
  • 8
  • [ 1070-62-8 ]
  • [ 110-94-1 ]
  • 9
  • [ 117903-19-2 ]
  • [ 110-94-1 ]
  • [ 64-17-5 ]
  • [ 1070-62-8 ]
  • [ 53594-71-1 ]
  • [ 67-63-0 ]
  • 10
  • [ 110-94-1 ]
  • [ 74-89-5 ]
  • [ 25077-25-2 ]
  • 11
  • [ 1004-38-2 ]
  • [ 110-94-1 ]
  • pyrimidine-2,4,6-triamine; compound with pentanedioic acid [ No CAS ]
  • 12
  • [ 818-38-2 ]
  • Al2O3 [ No CAS ]
  • [ 110-94-1 ]
  • [ 74-85-1 ]
  • [ 1070-62-8 ]
  • 14
  • [ 110-94-1 ]
  • [ 1070-62-8 ]
  • 15
  • [ 110-94-1 ]
  • cobalt(II) acetate [ No CAS ]
  • [ 151433-25-9 ]
  • [(1-RR)-(Glutaric acid)] [ No CAS ]
YieldReaction ConditionsOperation in experiment
100% 1.8 g of (R, R) -N,N'-bis (3, 5-di-t-butylsalicylidene) -1,2- cyclohexanediamine and 1.1 g of cobalt (II) acetate-4H2O were mixed in 35 ml of ethanol and stirred under reflux for 5 hours. They were filtered at room temperature and cleaned by small amount of ethanol. The obtained solid was uniformly divided into four parts and mixed with 6 ml of acetone and 10 ml of dichloromethane respectively. Also, 1.0 equivalent weight of succinic acid, glutaric acid, adipic acid, and pimeric acid were added respectively and stirred for 3 hours with injection of air at room temperature. After the solvent was eliminated under reduced pressure, the title compounds were obtained quantitatively.
  • 16
  • [ 110-94-1 ]
  • [ 173334-57-1 ]
  • aliskiren glutaric acid salt [ No CAS ]
YieldReaction ConditionsOperation in experiment
In ethanol; dichloromethane; at 20℃; for 24h; Example 23: Preparation of aliskiren glutaric acid salt <strong>[173334-57-1]Aliskiren</strong> (1.6 g, 2.9 mmol) was dissolved in dichloromethane (10 mL), and glutaric acid (0.191 g, 1.45 mmol) in ethanol (1 mL) was added while stirring. The solution was stirred at room temperature for 24 h. Then, the solvent was evaporated in vacuum and the product was dried under vacuum at 30C over night. Mp = 71.5-75.8C XRPD: amorphous
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