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. 301673-16-5 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 301673-16-5
Chemical Structure| 301673-16-5
Structure of 301673-16-5 * 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 [ 301673-16-5 ]

Related Doc. of [ 301673-16-5 ]

Alternatived Products of [ 301673-16-5 ]
Product Citations

Product Details of [ 301673-16-5 ]

CAS No. :301673-16-5 MDL No. :MFCD04115304
Formula : C10H20N2O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :-
M.W : 216.28 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 301673-16-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 64.47
TPSA : 61.8 ?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) : -7.73 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.4
Log Po/w (XLOGP3) : -0.16
Log Po/w (WLOGP) : -0.57
Log Po/w (MLOGP) : 0.03
Log Po/w (SILICOS-IT) : 0.01
Consensus Log Po/w : 0.34

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.82
Solubility : 33.0 mg/ml ; 0.153 mol/l
Class : Very soluble
Log S (Ali) : -0.68
Solubility : 44.9 mg/ml ; 0.208 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.88
Solubility : 28.2 mg/ml ; 0.131 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.9

Safety of [ 301673-16-5 ]

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

Application In Synthesis of [ 301673-16-5 ]

* 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 [ 301673-16-5 ]

[ 301673-16-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 207981-46-2 ]
  • [ 301673-16-5 ]
  • [ 1000782-05-7 ]
YieldReaction ConditionsOperation in experiment
67.0% With triethylamine; In tetrahydrofuran; at 10 - 30℃; for 1h; To a solution of tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1.00 g, 4.62 mmol) and triethylamine (0.967 ml, 6.94 mmol) in tetrahydrofuran (20 ml) was added 5-trifluoromethyl-2-fluorobenzoyl chloride (0.837 ml, 5.54 mmol) at room temperature, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the object product (1.26 g, 67.0%) as an oil. 1H-NMR (CDCl3) δ; 1.47 (9H, s), 3.02 (3H, br s), 3.29 (1H, br s), 3.61 (1H, br s), 3.79 (1H, br s), 4.08-4.22 (2H, br s), 4.51-4.54 (1H, m), 4.85 (1H, br s), 7.21-7.26 (1H, m), 7.68-7.72 (2H, m)
  • 2
  • [ 301673-16-5 ]
  • [ 171178-50-0 ]
  • [ 1000782-18-2 ]
YieldReaction ConditionsOperation in experiment
50.3% A mixture of <strong>[171178-50-0]2,6-difluoronicotinic acid</strong> (1.00 g, 6.28 mmol) and thionyl chloride (10 ml) was stirred at 85 C. for 2 hr, and the solvent was evaporated under reduced pressure. The residue was added to a solution of tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1.00 g, 4.62 mmol) and triethylamine (1.29 ml, 9.24 mmol) in tetrahydrofuran (10 ml) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give the object product (830 mg, 50.3%) as a solid. 1H-NMR (CDCl3) δ; 1.47 (9H, s), 3.01 (3H, br s), 3.31-3.38 (1H, m), 3.61 (1H, br s), 3.78 (1H, br s), 4.12 (2H, br s), 4.45-4.48 (1H, m), 4.82 (1H, br s), 6.90-6.96 (1H, m), 7.94-8.06 (1H, m).
  • 3
  • [ 129799-08-2 ]
  • [ 301673-16-5 ]
YieldReaction ConditionsOperation in experiment
83% With sodium tetrahydroborate; ethanol; nickel dichloride; at 0℃; for 4h;Inert atmosphere; To a mixture of 1-tert-butyl 3-methyl piperazine-1, 3-dicarboxylate (1.0 g, 4.1 mmol) , nickel chloride (640 mg, 4.9 mmol) and anhydrous ethanol (10 mL) was added sodium borohydride (380 mg, 10.0 mmol) at 0 . The mixture was stirred for 4 h and quenched with ice-water (5 mL) . The mixture was adjusted with concentrated hydrochloric acid to pH 1. After the mixture was clear, a NaOH aqueous solution (1.0 M) was added to adjust pH 10. The resulting mixture was extracted with EtOAc (10 mL × 3) . The combined organic layers were dried over anhydrous Na2SO4 and concentrated to give tert-butyl 3- (hydroxymethyl) piperazine-1-carboxylate as a reseda solid (890 mg, 83) .1H NMR (400 MHz, CD3OD) : delta ppm 3.99-4.02 (m, 1H) , 3.90-3.93 (m, 1H) , 3.48-3.54 (m, 2H) , 2.96-3.00 (m, 1H) , 2.83-2.93 (m, 1H) , 2.66-2.72 (m, 2H) , 2.56-2.66 (m, 1H) , 1.48 (m, 9H) and MS-ESI: m/z 217.10 [M+H] +.
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 301673-16-5 ]

Alcohols

Chemical Structure| 314741-40-7

[ 314741-40-7 ]

(S)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 278788-66-2

[ 278788-66-2 ]

(R)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 1030377-21-9

[ 1030377-21-9 ]

(S)-1-Boc-2-(Hydroxymethyl)piperazine

Similarity: 1.00

Chemical Structure| 169448-87-7

[ 169448-87-7 ]

(R)-tert-Butyl 2-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 205434-75-9

[ 205434-75-9 ]

1-Boc-(2-Hydroxymethyl)piperazine

Similarity: 1.00

Amides

Chemical Structure| 314741-40-7

[ 314741-40-7 ]

(S)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 278788-66-2

[ 278788-66-2 ]

(R)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 1030377-21-9

[ 1030377-21-9 ]

(S)-1-Boc-2-(Hydroxymethyl)piperazine

Similarity: 1.00

Chemical Structure| 169448-87-7

[ 169448-87-7 ]

(R)-tert-Butyl 2-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 205434-75-9

[ 205434-75-9 ]

1-Boc-(2-Hydroxymethyl)piperazine

Similarity: 1.00

Related Parent Nucleus of
[ 301673-16-5 ]

Aliphatic Heterocycles

Chemical Structure| 314741-40-7

[ 314741-40-7 ]

(S)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 278788-66-2

[ 278788-66-2 ]

(R)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 1030377-21-9

[ 1030377-21-9 ]

(S)-1-Boc-2-(Hydroxymethyl)piperazine

Similarity: 1.00

Chemical Structure| 169448-87-7

[ 169448-87-7 ]

(R)-tert-Butyl 2-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 205434-75-9

[ 205434-75-9 ]

1-Boc-(2-Hydroxymethyl)piperazine

Similarity: 1.00

Piperazines

Chemical Structure| 314741-40-7

[ 314741-40-7 ]

(S)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 278788-66-2

[ 278788-66-2 ]

(R)-tert-Butyl 3-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 1030377-21-9

[ 1030377-21-9 ]

(S)-1-Boc-2-(Hydroxymethyl)piperazine

Similarity: 1.00

Chemical Structure| 169448-87-7

[ 169448-87-7 ]

(R)-tert-Butyl 2-(hydroxymethyl)piperazine-1-carboxylate

Similarity: 1.00

Chemical Structure| 205434-75-9

[ 205434-75-9 ]

1-Boc-(2-Hydroxymethyl)piperazine

Similarity: 1.00

; ;