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. 552-41-0 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 552-41-0
Chemical Structure| 552-41-0
Structure of 552-41-0 * 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 [ 552-41-0 ]

Related Doc. of [ 552-41-0 ]

Alternatived Products of [ 552-41-0 ]
Product Citations

Product Citations

Han, Guanqun ;

Abstract: Mankind's sustainable development not only requires the capture and conversion of renewable energies but also necessitates the production of chemical goods from renewable carbon sources. Biomass is the only accessible and renewable carbon source. One major class of biomass is degradative small molecules, among which 5-hydroxymethylfurfural (HMF) is considered as a platform chemical and it can serve as a starting material to produce various upgrading compounds, eg, the oxidation products, 2, 5-furan dicarboxylic acid (FDCA), and 2, 5-diformylfuran (DFF), can act as biopolymer precursors. In this dissertation, we successfully demonstrated that ultrathin Ni/CdS nanosheets can be efficient photocatalyst to produce value-added bioproducts (eg, furoic acid, DFF, and FDCA) from biomass-derived molecules. Even more desirable is that the oxidative biomass upgrading can be integrated with H2 production.

Purchased from AmBeed: ; ; ; ; ; ;

Product Details of [ 552-41-0 ]

CAS No. :552-41-0 MDL No. :MFCD00008730
Formula : C9H10O3 Boiling Point : -
Linear Structure Formula :HOC6H2(OCH3)(CH3)CHO InChI Key :UILPJVPSNHJFIK-UHFFFAOYSA-N
M.W : 166.17 Pubchem ID :11092
Synonyms :
2'-Hydroxy-4'-methoxyacetophenone;Peonol;NSC 401442
Chemical Name :1-(2-Hydroxy-4-methoxyphenyl)ethanone

Calculated chemistry of [ 552-41-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 45.15
TPSA : 46.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.06
Log Po/w (XLOGP3) : 1.98
Log Po/w (WLOGP) : 1.6
Log Po/w (MLOGP) : 0.83
Log Po/w (SILICOS-IT) : 1.68
Consensus Log Po/w : 1.63

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.36
Solubility : 0.733 mg/ml ; 0.00441 mol/l
Class : Soluble
Log S (Ali) : -2.58
Solubility : 0.434 mg/ml ; 0.00261 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.28
Solubility : 0.876 mg/ml ; 0.00527 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.28

Safety of [ 552-41-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P273-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335-H412 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 552-41-0 ]

* 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 [ 552-41-0 ]

[ 552-41-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 552-41-0 ]
  • [ 28090-12-2 ]
  • [ 943860-45-5 ]
  • 2
  • [ 552-41-0 ]
  • [ 30992-63-3 ]
  • 3
  • [ 552-41-0 ]
  • [ 97-08-5 ]
  • C15H12ClNO7S [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% With triethylamine; In dichloromethane; at 20℃; General procedure: To a solution of paeonol/2-hydroxy acetophenone/3-methoxyphenol (1/2/3, 1.0 mmol) and ethanesulfonyl chloride/arylsulfonyl chloride (7, 1.2 mmol) in dry dichloromethane (CH2Cl2, 10 ml) at room temperature, a solution of triethylamine (Et3N) (1.5 mmol) in dry CH2Cl2 (5 ml) was added dropwise for 10 min. When the reaction was completed by TLC analysis, the reaction mixture was diluted with water (15 ml), and extracted with CH2Cl2 (30 ml*3). Subsequently, the combined organic phasewas washed by saturated aq. brine (30 ml), dried over anhydrous Na2SO4, concentrated in vacuo, and purified by silica gel column chromatography to obtain title compounds. The data for 4a-p, 5a-p, and 6a-p are shown as follows.
  • 4
  • [ 552-41-0 ]
  • [ 2150-11-0 ]
Recommend Products
Same Skeleton Products

Technical Information

Historical Records
; ;