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[ CAS No. 2516-97-4 ] {[proInfo.proName]}

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Chemical Structure| 2516-97-4
Chemical Structure| 2516-97-4
Structure of 2516-97-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2516-97-4 ]

CAS No. :2516-97-4 MDL No. :MFCD00051843
Formula : C3H6O4S Boiling Point : -
Linear Structure Formula :- InChI Key :NYEHUAQIJXERLP-UHFFFAOYSA-N
M.W : 138.14 Pubchem ID :3732841
Synonyms :

Calculated chemistry of [ 2516-97-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 27.27
TPSA : 79.82 ?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) : -7.71 cm/s

Lipophilicity

Log Po/w (iLOGP) : -0.12
Log Po/w (XLOGP3) : -0.8
Log Po/w (WLOGP) : 0.2
Log Po/w (MLOGP) : -1.09
Log Po/w (SILICOS-IT) : -0.79
Consensus Log Po/w : -0.52

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -0.06
Solubility : 120.0 mg/ml ; 0.87 mol/l
Class : Very soluble
Log S (Ali) : -0.4
Solubility : 55.3 mg/ml ; 0.401 mol/l
Class : Very soluble
Log S (SILICOS-IT) : 0.06
Solubility : 158.0 mg/ml ; 1.14 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 2516-97-4 ]

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 [ 2516-97-4 ]

* 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 [ 2516-97-4 ]

[ 2516-97-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2516-97-4 ]
  • [ 1131-52-8 ]
  • [ 253168-94-4 ]
YieldReaction ConditionsOperation in experiment
78% With thionyl chloride; ammonium acetate; In ethanol; for 16h;Reflux; Add 500 ml of ethanol to a 500 ml three-necked flask, 12.4 g of 2- (methylsulfonyl) acetic acid and 18.2 g of ammonium acetate, heated to 50 C,10.0 g of 3-ethoxy-4-methoxybenzaldehyde was added dropwise, heating reflux reaction. Cooled to below 10C, 40 g of thionyl chloride was added dropwise and heated under reflux for 16 hours to distill off ethanol. To the residue was added 50 ml of dichloromethane and the pH was adjusted to 6-7 with 5 mol / L NaOH solution.The organic layer was separated and the aqueous layer was extracted with dichloromethane. The organic layers were combined and concentrated to give 14.2 g of a colorless oil,HPLC purity 98%, yield 78%.
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