- Discovery of 2-substituted 1H-benzo[d]imidazole-4-carboxamide derivatives as novel poly(ADP-ribose)polymerase-1 inhibitors with in vivo anti-tumor activityZhou, Jie; Ji, Ming; Zhu, Zhixiang; Cao, Ran; Chen, Xiaoguang; et al, European Journal of Medicinal Chemistry, 2017, 132, 26-41
Cas no 959237-16-2 (tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate)
959237-16-2 structure
Product Name:tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate
CAS No:959237-16-2
MF:C15H29N3O2
MW:283.409663915634
MDL:MFCD09864242
CID:1988441
PubChem ID:53415311
Update Time:2025-09-20
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate Chemical and Physical Properties
Names and Identifiers
-
- Tert-butyl 4-(4-aminopiperidin-1-yl)piperidine-1-carboxylate
- SureCN4161964
- AM804618
- A25955
- B-1383
- tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate
- F2167-0878
- tert-butyl 4-amino-[1,4'-bipiperidine]-1'-carboxylate
- 1,1-Dimethylethyl 4-amino[1,4′-bipiperidine]-1′-carboxylate (ACI)
- DTXSID00697035
- AS-68869
- tert-butyl 4-(4-aMinopiperidin-1-yl)
- tert-Butyl 4-amino[1,4'-bipiperidine]-1'-carboxylate
- EN300-240388
- DB-080367
- Z1505698968
- 959237-16-2
- tert-Butyl4-amino-1,4'-bipiperidine-1'-carboxylate
- 1'-Boc-4-amino-[1,4'-bipiperidine]
- MFCD09864242
- AKOS007930561
- W15140
- SY124095
- CS-0036248
- tert-butyl4-amino-[1,4'-bipiperidine]-1'-carboxylate
- 1 inverted exclamation mark -Boc-[1,4 inverted exclamation mark -bipiperidin]-4-amine
- SCHEMBL4161964
-
- MDL: MFCD09864242
- Inchi: 1S/C15H29N3O2/c1-15(2,3)20-14(19)18-10-6-13(7-11-18)17-8-4-12(16)5-9-17/h12-13H,4-11,16H2,1-3H3
- InChI Key: AHAQZBVUGZUUMB-UHFFFAOYSA-N
- SMILES: O=C(N1CCC(N2CCC(N)CC2)CC1)OC(C)(C)C
Computed Properties
- Exact Mass: 283.22597718g/mol
- Monoisotopic Mass: 283.22597718g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 20
- Rotatable Bond Count: 4
- Complexity: 325
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.3
- Topological Polar Surface Area: 58.8?2
Experimental Properties
- Density: 1.075
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-XD022-200mg |
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate |
959237-16-2 | 95+% | 200mg |
815.0CNY | 2021-07-14 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-XD022-50mg |
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate |
959237-16-2 | 95+% | 50mg |
406.0CNY | 2021-07-14 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-XD022-1g |
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate |
959237-16-2 | 95+% | 1g |
2446.0CNY | 2021-07-14 | |
| Chemenu | CM323273-250mg |
tert-Butyl 4-amino-[1,4'-bipiperidine]-1'-carboxylate |
959237-16-2 | 95% | 250mg |
$158 | 2022-08-31 | |
| Chemenu | CM323273-1g |
tert-Butyl 4-amino-[1,4'-bipiperidine]-1'-carboxylate |
959237-16-2 | 95% | 1g |
$392 | 2022-08-31 | |
| Chemenu | CM323273-5g |
tert-Butyl 4-amino-[1,4'-bipiperidine]-1'-carboxylate |
959237-16-2 | 95% | 5g |
$1081 | 2022-08-31 | |
| abcr | AB215573-1 g |
tert-Butyl4-amino-1,4'-bipiperidine-1'-carboxylate; 95% |
959237-16-2 | 1g |
€356.30 | 2022-03-04 | ||
| eNovation Chemicals LLC | Y1189531-1g |
1'-Boc-[1,4'-bipiperidin]-4-amine |
959237-16-2 | 95% | 1g |
$1380 | 2023-09-01 | |
| eNovation Chemicals LLC | D772609-100mg |
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate |
959237-16-2 | 95% | 100mg |
$75 | 2024-06-06 | |
| eNovation Chemicals LLC | D772609-250mg |
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate |
959237-16-2 | 95% | 250mg |
$100 | 2024-06-06 |
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: 1,1,1,3,3,3-Hexafluoro-2-propanol ; 20 h, 1 atm, rt
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Ammonium formate , Ammonia Catalysts: Palladium Solvents: Methanol ; overnight, rt
Reference
- Preparation of triazole derivatives with antifungal activity, World Intellectual Property Organization, , ,
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate Raw materials
- tert-Butyl 4-oxo-1,4'-bipiperidine-1'-carboxylate
- t-Butyl 4-(benzyloxycarbonylamino)-1,4'-bipiperidine-1'-carboxylate
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate Preparation Products
tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate Related Literature
-
Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
-
3. An integrated microfluidic 3D tumor system for parallel and high-throughput chemotherapy evaluation?Dan Liu,Rui Hu,Zhongchao Huang,Meilin Sun,Kai Han Analyst, 2020,145, 6447-6455
-
Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
-
José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
959237-16-2 (tert-butyl 4-amino-1,4'-bipiperidine-1'-carboxylate) Related Products
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