成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart 0 Sign in  

[ CAS No. 5355-68-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 5355-68-0
Chemical Structure| 5355-68-0
Structure of 5355-68-0 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 5355-68-0 ]

Related Doc. of [ 5355-68-0 ]

Alternatived Products of [ 5355-68-0 ]
Product Citations

Product Details of [ 5355-68-0 ]

CAS No. :5355-68-0 MDL No. :MFCD00038035
Formula : C8H15NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :CCDBCHAQIXKJCG-UHFFFAOYSA-N
M.W : 141.21 Pubchem ID :79313
Synonyms :

Calculated chemistry of [ 5355-68-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.47
TPSA : 20.31 ?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) : -6.79 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 0.52
Log Po/w (WLOGP) : 0.68
Log Po/w (MLOGP) : 0.76
Log Po/w (SILICOS-IT) : 1.51
Consensus Log Po/w : 1.09

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.98
Solubility : 14.9 mg/ml ; 0.105 mol/l
Class : Very soluble
Log S (Ali) : -0.52
Solubility : 42.9 mg/ml ; 0.304 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.29
Solubility : 7.24 mg/ml ; 0.0513 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.02

Safety of [ 5355-68-0 ]

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

Application In Synthesis of [ 5355-68-0 ]

* 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 [ 5355-68-0 ]

[ 5355-68-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5355-68-0 ]
  • [ 186534-02-1 ]
  • 3,5-bis(3,5,6-trimethylpyrazin-2-ylmethylene)-1-isopropylpiperidin-4-one oxime [ No CAS ]
  • 2
  • [ 5355-68-0 ]
  • [ 186534-02-1 ]
  • 3,5-bis-(3,5,6-trimethylpyrazin-2-ylmethylene)-1-isopropylpiperidin-4-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
59% With sodium hydroxide; In ethanol; at 5 - 27℃; General procedure: New a, b-unsaturated carbonyl-based compounds (5a-g and 6au)were synthesized using direct coupling technique [40] (Scheme 1). The reaction was carried out using base-catalyzed Claisen-Schmidt condensation reaction, by reacting different types of ketoneswith appropriate aromatic aldehyde at molar ratio 2:1 tosynthesize new compounds (5a-g) and at molar ratio 1:1 for (6a-u).For synthesis of 6a-u first 5a-g intermediates were synthesized andin second step appropriate aldehydes were reacted with intermediates.The detailed method of synthesis has already beenreported by us previously [38,40]. Scheme 1 shows the highlights ofsynthesis of compound 3, 4 and a, b-unsaturated carbonyl-basedcompounds along with oxime derivatives. 15 mL ethanol wastaken in a round bottom flask and aromatic aldehyde (20 mmol, 2equivalent) and specific ketone (10 mmol,1 equivalent) were addedand dissolved using a stirrer for 2-3 min at 5 C. Into the abovesolution, 40% NaOH solution in ethanol was added drop wise andthe mixture was stirred for 1-24 h at 27 C. The color change andprecipitate formation in the reaction mixture showed productformation. TLC was used to monitor the reaction and acidified icewas added to quench the reaction once completed. The isolation ofcompounds was done by recrystallization and/or by using columnchromatography.
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 5355-68-0 ]

Ketones

Chemical Structure| 1445-73-4

[ 1445-73-4 ]

1-Methyl-4-piperidone

Similarity: 0.92

Chemical Structure| 532-24-1

[ 532-24-1 ]

8-Methyl-8-azabicyclo[3.2.1]octan-3-one

Similarity: 0.90

Chemical Structure| 77542-18-8

[ 77542-18-8 ]

1-Ethyl-1-methyl-4-oxopiperidin-1-ium iodide

Similarity: 0.89

Chemical Structure| 72544-16-2

[ 72544-16-2 ]

1-Isobutylpiperidin-4-one

Similarity: 0.86

Chemical Structure| 1245645-90-2

[ 1245645-90-2 ]

2-Propylpiperidin-4-one hydrochloride

Similarity: 0.83

Related Parent Nucleus of
[ 5355-68-0 ]

Piperidines

Chemical Structure| 1445-73-4

[ 1445-73-4 ]

1-Methyl-4-piperidone

Similarity: 0.92

Chemical Structure| 77542-18-8

[ 77542-18-8 ]

1-Ethyl-1-methyl-4-oxopiperidin-1-ium iodide

Similarity: 0.89

Chemical Structure| 72544-16-2

[ 72544-16-2 ]

1-Isobutylpiperidin-4-one

Similarity: 0.86

Chemical Structure| 1245645-90-2

[ 1245645-90-2 ]

2-Propylpiperidin-4-one hydrochloride

Similarity: 0.83

Chemical Structure| 41979-39-9

[ 41979-39-9 ]

Piperidin-4-one hydrochloride

Similarity: 0.81

; ;