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125541-22-2

125541-22-2 Structure

125541-22-2 Structure
IdentificationBack Directory
[Name]

1-N-Boc-4-(Phenylamino)piperidine
[CAS]

125541-22-2
[Synonyms]

4-(phenylamino)-
Aniline piperidine
1-N-Boc-4-(Phenylami
(Phenylamino)piperidine
1-N-Boc-4-(Phenylamino)
99%1,1-dimethylethyl ester
4-Anilino-1-Boc-piperidine
1-N-Boc-4-anilinopiperidine
1-N-Boc-4- aniline piperidine
1-Boc-4-(phenylaMino)piperidine
-N-Boc-4-(Phenylamino)Piperidine
1 -N-Boc-4-(Phenylamino)piperidin
1-N-BOC-4-(PHENYLAMINO)PIPERIDINE
L-Carnitine/ Orlistat/ Rasagiline
Intermediate for Fentanyl derivatives
ethyl 6-bromo-4-[(dimethylamino)methyl]
1-N-Boc-4-(Phenylamino)piperidine - 97.0%
N-tert-Butoxycarbonyl-4-anilinopiperidine
1-N-Boc-4-(Phenylamino)piperidine Supplier
4-(Phenylamino)piperidine, N1-BOC protected
4-(Phenylamino)piperidine,N1-BOCprotected95%
tert-butyl 4-anilinopiperidine-1-carboxylate
1-(tert-Butoxycarbonyl)-4-phenylaminopiperidine
1-N-Boc-4-(Phenylamino)piperidine CAS 125541-22-2
tert-butyl 4-(phenylaMino)piperidine-1-carboxylate
1-(tert-Butyloxycarbonyl)-4-(phenylaMino)piperidine
1-N-Boc-4-(Phenylamino)piperidine Basic information
ethyl 3-oxo-2-phenylbutanoate(BMK)(BMK glycidate oil)
2-Methyl-2-propanyl 4-anilino-1-piperidinecarboxylate
C16H24N2O2 tert-Butyl 4-anilinopiperidine-1-carboxylate
TERT-BUTYL 4-ANILINOTETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE
Widely Used 99% 1-N-Boc-4- (Phenylamino) Piperidine Powder
High purity 1-N-Boc-4-(Phenylamino)piperidine CAS 125541-22-2
tert-butyl 4-anilinotetrahydro-1(2H)-pyridinecarboxylate (en)
CAS 125541-22-2 Pharmaceutical/1-N-Boc-4- (Phenylamino) Piperidine
4-(PhenylaMino)-1-piperidinecarboxylic Acid 1,1-DiMethylethyl Ester
1-N-Boc-4-(Pheny 1-N-Boc-4-(Phenylamino)piperidinelamino)piperidine
1-Piperidinecarboxylicacid, 4-(phenylaMino)-, 1,1-diMethylethyl ester
tert-Butyl 4-(phenylamino)piperidine-1-carboxylate, tert-Butyl 4-anilinopiperidine-1-carboxylate
[EINECS(EC#)]

203-105-0
[Molecular Formula]

C16H24N2O2
[MDL Number]

MFCD02102489
[MOL File]

125541-22-2.mol
[Molecular Weight]

276.37
Chemical PropertiesBack Directory
[Melting point ]

136-137
[Boiling point ]

400.6±38.0 °C(Predicted)
[density ]

1.107±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMF: 15mg/mL; DMSO: 25mg/mL; Ethanol: 25mg/mL; Ethanol:PBS (pH 7.2) (1:1): 0.5mg/mL
[form ]

A crystalline solid
[pka]

5.00±0.20(Predicted)
[InChI]

InChI=1S/C16H24N2O2/c1-16(2,3)20-15(19)18-11-9-14(10-12-18)17-13-7-5-4-6-8-13/h4-8,14,17H,9-12H2,1-3H3
[InChIKey]

HTIWISWAPVQGMI-UHFFFAOYSA-N
[SMILES]

N1(C(OC(C)(C)C)=O)CCC(NC2=CC=CC=C2)CC1
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[Hazard Note ]

Harmful/Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Description]

4-Anilino-1-Boc-piperidine (Item No. 29119) is an analytical reference standard that is structurally similar to known opioids. 4-Anilino-1-Boc-piperidine is a precursor in the synthesis of 4-anilinopiperidine (Item No. 20085). This product is intended for research and forensic applications.
[Chemical Properties]

Pale Brown Solid
[Uses]

Intermediate in the preparation of Fentanyl derivatives.
[Application]

1-N-Boc-4-(Phenylamino)piperidine is an amino acid derivative widely employed as a reagent in organic synthesis. This compound exhibits remarkable versatility, finding applications in various fields such as peptide and protein synthesis, organic synthesis, and drug development. It possesses strong basic properties, allowing for diverse reactions with acids that lead to the formation of a wide array of products. The extensive use of this compound in organic synthesis is well-documented, particularly in the synthesis of peptides and proteins. By facilitating the coupling of amino acids, it enables the creation of peptides that can be utilized in diverse applications, including the development of pharmaceutical drugs.
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