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. 114214-69-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 114214-69-6
Chemical Structure| 114214-69-6
Structure of 114214-69-6 * 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 [ 114214-69-6 ]

Related Doc. of [ 114214-69-6 ]

Alternatived Products of [ 114214-69-6 ]
Product Citations

Product Details of [ 114214-69-6 ]

CAS No. :114214-69-6 MDL No. :MFCD02179040
Formula : C10H19NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :HKIGXXRMJFUUKV-UHFFFAOYSA-N
M.W : 201.26 Pubchem ID :5237175
Synonyms :
Chemical Name :tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate

Calculated chemistry of [ 114214-69-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 57.75
TPSA : 49.77 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.45
Log Po/w (XLOGP3) : 0.82
Log Po/w (WLOGP) : 0.85
Log Po/w (MLOGP) : 0.86
Log Po/w (SILICOS-IT) : 0.65
Consensus Log Po/w : 1.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.34
Solubility : 9.19 mg/ml ; 0.0457 mol/l
Class : Very soluble
Log S (Ali) : -1.45
Solubility : 7.19 mg/ml ; 0.0357 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.83
Solubility : 29.8 mg/ml ; 0.148 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.65

Safety of [ 114214-69-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P273-P301+P310-P391-P405 UN#:2811
Hazard Statements:H301-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 114214-69-6 ]

* 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 [ 114214-69-6 ]

[ 114214-69-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 114214-69-6 ]
  • [ 305329-97-9 ]
YieldReaction ConditionsOperation in experiment
55% With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 18h; To a solution of 1 ,1 -dimethylethyl 3-(hydroxymethyl)-1 - pyrrolidinecarboxylate (0.56 g, 2.8 mmol) with carbon tetrabromide (1.39 g, 4.2 mmol) in methylene chloride (10 ml_) was added drop wise a solution of triphenyl phosphine (0.73 g, 2.8 mmol in 5 mL of methylene chloride). Upon completion the mixture was stirred 18 h at room temperature. The solvent was removed at reduced pressure and the residue stirred in 10% ethyl acetate 90% hexane. The <n="54"/>mixture was filtered and the resulting solution chromatographed on silica eluting with a gradient of 0 - 25% EtOAc in hexane to afford the desired compound (0.41 g, 55%). MS (ES+) m/z 264 (M+H)+.
55% With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 20℃; for 18h; To a solution of 1 ,1-dimethylethyl 3-(hydroxymethyl)-1-pyrrolidinecarboxylate (0.56 g, 2.8 mmol) with carbon tetrabromide (1.39 g, 4.2 mmol) in methylene chloride (10 ml.) was added drop wise a solution of triphenyl phosphine (0.73 g, 2.8 mmol in 5 ml. of methylene chloride). Upon completion the mixture was stirred 18 h at room temperature. The solvent was removed at reduced pressure and the residue stirred in 10% ethyl acetate 90% hexane. The mixture was filtered and the resulting solution chromatographed on silica eluting with a gradient of 0 - 25% EtOAc in hexane to afford the desired compound (0.41 g, 55%). MS (ES+) m/z 264 (M+H)+.
  • 2
  • [ 114214-69-6 ]
  • [ 138108-72-2 ]
  • [ 199174-24-8 ]
YieldReaction ConditionsOperation in experiment
73% Resolution of racemate; Racemic l-t-butoxycarbonylpyrrolidine-3-methanol (15 g,74.53 mmol) was chromatographed on a chiral column[ChiralPak AD 8 X 25 cm; 2.5% of (6% MeOH/94% EtOH); 400mL/min; UV: 210 nm] to give l-t-butoxycarbonylpyrrolidine-3-methanol:Isomer I (Rt: 8.81 min, ChiralPak AD 4.6 X 250 mm; 1.0mL/min; UV: 210 nm) (6.35 g, 42%, 94% ee) andIsomer II (Rt: 9.68 min)' (6.43 g, 43%, 90% ee) .Isomer I: FIA-MS, m/e: 202.2 (rrH-1) .Isomer II: FIA-MS, m/e: 202.2 (m+1).
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 114214-69-6 ]

Alcohols

Chemical Structure| 199174-24-8

[ 199174-24-8 ]

(S)-1-Boc-(3-Hydroxymethyl)pyrrolidine

Similarity: 1.00

Chemical Structure| 138108-72-2

[ 138108-72-2 ]

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

Similarity: 1.00

Chemical Structure| 663172-78-9

[ 663172-78-9 ]

N-Boc-6-hydroxy-3-azabicyclo[3.2.0]heptane

Similarity: 0.94

Chemical Structure| 116574-71-1

[ 116574-71-1 ]

tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate

Similarity: 0.94

Chemical Structure| 140695-84-7

[ 140695-84-7 ]

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

Similarity: 0.94

Amides

Chemical Structure| 199174-24-8

[ 199174-24-8 ]

(S)-1-Boc-(3-Hydroxymethyl)pyrrolidine

Similarity: 1.00

Chemical Structure| 138108-72-2

[ 138108-72-2 ]

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

Similarity: 1.00

Chemical Structure| 663172-78-9

[ 663172-78-9 ]

N-Boc-6-hydroxy-3-azabicyclo[3.2.0]heptane

Similarity: 0.94

Chemical Structure| 116574-71-1

[ 116574-71-1 ]

tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate

Similarity: 0.94

Chemical Structure| 140695-84-7

[ 140695-84-7 ]

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

Similarity: 0.94

Related Parent Nucleus of
[ 114214-69-6 ]

Aliphatic Heterocycles

Chemical Structure| 199174-24-8

[ 199174-24-8 ]

(S)-1-Boc-(3-Hydroxymethyl)pyrrolidine

Similarity: 1.00

Chemical Structure| 138108-72-2

[ 138108-72-2 ]

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

Similarity: 1.00

Chemical Structure| 663172-78-9

[ 663172-78-9 ]

N-Boc-6-hydroxy-3-azabicyclo[3.2.0]heptane

Similarity: 0.94

Chemical Structure| 116574-71-1

[ 116574-71-1 ]

tert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylate

Similarity: 0.94

Chemical Structure| 140695-84-7

[ 140695-84-7 ]

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

Similarity: 0.94

Pyrrolidines

Chemical Structure| 199174-24-8

[ 199174-24-8 ]

(S)-1-Boc-(3-Hydroxymethyl)pyrrolidine

Similarity: 1.00

Chemical Structure| 138108-72-2

[ 138108-72-2 ]

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

Similarity: 1.00

Chemical Structure| 199175-10-5

[ 199175-10-5 ]

(S)-1-Boc-3-(Aminomethyl)pyrrolidine

Similarity: 0.92

Chemical Structure| 274692-08-9

[ 274692-08-9 ]

(S)-tert-Butyl 3-(2-aminoethyl)pyrrolidine-1-carboxylate

Similarity: 0.92

Chemical Structure| 270912-72-6

[ 270912-72-6 ]

tert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylate

Similarity: 0.92

; ;