天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Home Cart 0 Sign in  

[ CAS No. 1092522-02-5 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1092522-02-5
Chemical Structure| 1092522-02-5
Structure of 1092522-02-5 * 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 [ 1092522-02-5 ]

Related Doc. of [ 1092522-02-5 ]

Alternatived Products of [ 1092522-02-5 ]
Product Citations

Product Details of [ 1092522-02-5 ]

CAS No. :1092522-02-5 MDL No. :MFCD10693199
Formula : C12H18N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :CPTVSMDBNANEBP-UHFFFAOYSA-N
M.W : 222.28 Pubchem ID :14139169
Synonyms :

Calculated chemistry of [ 1092522-02-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.42
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 65.99
TPSA : 55.56 ?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) : -6.24 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.53
Log Po/w (XLOGP3) : 1.99
Log Po/w (WLOGP) : 2.65
Log Po/w (MLOGP) : 2.07
Log Po/w (SILICOS-IT) : 0.89
Consensus Log Po/w : 2.03

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.49
Solubility : 0.727 mg/ml ; 0.00327 mol/l
Class : Soluble
Log S (Ali) : -2.78
Solubility : 0.366 mg/ml ; 0.00165 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.67
Solubility : 0.476 mg/ml ; 0.00214 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.06

Safety of [ 1092522-02-5 ]

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

Application In Synthesis of [ 1092522-02-5 ]

* 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 [ 1092522-02-5 ]

[ 1092522-02-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20291-40-1 ]
  • [ 1092522-02-5 ]
  • C20H30N2O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20℃; for 12h; General procedure: HBTU (1.82g, 3.59mmol), DIPEA (0.84mL, 4.80mmol) and monomethyl suberate (0.93mL, 5.28mmol) were added to a solution of 34 (1.0g, 4.80mmol) in DMF (10mL) and the mixture was stirred for 12hat rt. Then the reaction was quenched with H2O and extracted using EtOAc, dried over MgSO4 and passed through a filter column to give corresponding ester which was dissolved in the minimum amount of dioxane. H2O with pH adjusted to 3 using 3N HCl was added and the reaction mixture was stirred at reflux overnight to yield the corresponding free amine. The reaction was basified and extracted using EtOAc, then dried, concentrated and passed through a filter column to give the free amine. To a solution of this free amine (1.0g, 3.59mmol) in DMF (10mL) was added HBTU (1.36g, 3.59mmol), DIPEA (0.66mL, 3.59mmol) and 1,4-dibenzyloxy-5-isopropyl benzoic acid (0.76g, 4.31mmol) and the solution was stirred for 12hat 80C. The reaction mixture was quenched with H2O and extracted with EtOAc (25mL×3). The combined organic layer was collected, dried over anhydrous MgSO4 and concentrated under reduced pressure to give a light yellow residue, which was purified by silica gel chromatography (EtOAc:n-hexane=1: 1) to give 42 as a colorless liquid in 65% yield (overall from 34)
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 1092522-02-5 ]

Aryls

Chemical Structure| 528882-16-8

[ 528882-16-8 ]

3-(N-Tert-butoxycarbonyl-N-methylamino)aniline

Similarity: 0.98

Chemical Structure| 1160436-95-2

[ 1160436-95-2 ]

tert-Butyl (3-(dimethylamino)phenyl)carbamate

Similarity: 0.95

Chemical Structure| 71026-66-9

[ 71026-66-9 ]

tert-Butyl (4-aminophenyl)carbamate

Similarity: 0.93

Chemical Structure| 68621-88-5

[ 68621-88-5 ]

tert-Butyl (3-aminophenyl)carbamate

Similarity: 0.91

Chemical Structure| 1134328-09-8

[ 1134328-09-8 ]

tert-Butyl (3-(methylamino)phenyl)carbamate

Similarity: 0.91

Amides

Chemical Structure| 528882-16-8

[ 528882-16-8 ]

3-(N-Tert-butoxycarbonyl-N-methylamino)aniline

Similarity: 0.98

Chemical Structure| 1160436-95-2

[ 1160436-95-2 ]

tert-Butyl (3-(dimethylamino)phenyl)carbamate

Similarity: 0.95

Chemical Structure| 71026-66-9

[ 71026-66-9 ]

tert-Butyl (4-aminophenyl)carbamate

Similarity: 0.93

Chemical Structure| 68621-88-5

[ 68621-88-5 ]

tert-Butyl (3-aminophenyl)carbamate

Similarity: 0.91

Chemical Structure| 1134328-09-8

[ 1134328-09-8 ]

tert-Butyl (3-(methylamino)phenyl)carbamate

Similarity: 0.91

Amines

Chemical Structure| 528882-16-8

[ 528882-16-8 ]

3-(N-Tert-butoxycarbonyl-N-methylamino)aniline

Similarity: 0.98

Chemical Structure| 1160436-95-2

[ 1160436-95-2 ]

tert-Butyl (3-(dimethylamino)phenyl)carbamate

Similarity: 0.95

Chemical Structure| 71026-66-9

[ 71026-66-9 ]

tert-Butyl (4-aminophenyl)carbamate

Similarity: 0.93

Chemical Structure| 68621-88-5

[ 68621-88-5 ]

tert-Butyl (3-aminophenyl)carbamate

Similarity: 0.91

Chemical Structure| 1134328-09-8

[ 1134328-09-8 ]

tert-Butyl (3-(methylamino)phenyl)carbamate

Similarity: 0.91

; ;