| Name | N-Boc-Piperidine-4-carboxylic acid methyl ester |
|---|---|
| Synonyms |
MethylN-Boc-4-piperidinecboxylateG
4-Methyl 1-(2-methyl-2-propanyl) 1,4-piperidinedicarboxylate PIPERIDINE-1,4-DICBOXYLIC ACID 1-TERT-BUTYL ESTER 4-METHYL ESTER METHYL N-BOC-PIPERIDIN-4-CBOXYLATE Methyl 1-N-Boc-4-piperidinecboxylate 1-(1,1-Dimethylethyl) 4-methyl 1,4-piperidinedicboxylate 1-Boc-Piperidine-4-cboxylic acid methyl ester Methyl 1-Boc-4-piperidinecarboxylate Methyl 1-(tert-Butoxycbonyl)-4-piperidinecboxylate tert-Butyl Methyl piperidine-1,5-dicboxylate O1-tert-butyl O4-methyl piperidine-1,4-dicboxylate N-BOC-Piperidine-4-cboxylicacidmethyl N-boc-4-methylpiperidinate 1-(tert-butyl) 4-methyl tetrahydro-1,4(2H)-pyridinedicboxylate piperidine-1,4-dicboxylic acid O1-tert-butyl O4-methyl ester Methyl1-tert-butoxycbonylpiperidine-4-cboxyla MFCD02183584 N-Boc-Piperidine-4-cboxylate or 1-N-BOC-4-piperidinecboxylic acid Methyl ester Methyl 1-Boc-4-piperidinecboxylate 1,4-Piperidinedicarboxylic acid, 1-(1,1-dimethylethyl) 4-methyl ester N-BOC-PIPERIDINE-4-CBOXYLIC ACID METHYL ESTER Methyl piperidine-4-cboxylate, N-BOC protected 1-tert-butyl-4-methylpiperidin-1,4-dicarboxylat 1-tert-Butyl 4-methyl piperidine-1,4-dicboxylate, 1-(tert-Butoxycbonyl)-4-(methoxycbonyl)piperidine 1-N-BOC-4-PIPERIDINECBOXYLIC ACID METHYL ESTER N-Boc-Isonipecotic acid methyl ester 1-(tert-Butoxycbonyl)-4-piperidinecboxylic Acid Methyl Ester Methyl N-Boc-4-piperidinecboxylate Piperidine-1,4-dicboxylic Acid 1-tert-Butyl 4-Methyl 1-O-tert-butyl 4-O-methyl piperidine-1,4-dicboxylate 1,4-Piperidinedicboxylic acid, 1-(1,1-dimethylethyl) 4-methyl ester 1-Boc-4-piperidinecboxylic Acid Methyl Ester Methyl 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylate N-Boc-Piperidine-4-cboxyL 1-tert-butyl 4-methyl piperidine-1,4-dicarboxylate 1-[(tert-butoxy)carbonyl]-4-Methylpiperidine-2-cboxylate ic acid methyL methyl 1-boc-piperidine-4-carboxylate Methyl N-Boc-piperidine-4-cboxylate N-BOC-4-METHYL PIPERIDINECBOXYLATE 1-Boc-4-piperidinecboxylic Acid Methyl Ester 1-(tert-Butoxycbonyl)-4-piperidinecboxylic Acid Methyl Ester 1-tert-Butyl 4-Methyl Piperidine-1,4-dicboxylate Methyl 1-Boc-4-piperidinecboxylate N-Boc-piperidine-4-cboxylate, methyl ester N-Boc-Piperidine-4-Cboxylic Aacid Methyl Ester Methyl-boc-piperidine-4-cboxylate Methyl N-Boc-piperidine-4-carboxylate N-Boc- Piperidine-4-cboxylate 1-Boc-4-piperidinecarboxylic Acid Methyl Ester Piperidine-1,4-dicarboxylic Acid 1-tert-Butyl 4-Methyl Ester N-Boc-4-Methylpiperidine 1-O-tert-butyl 4-O-methyl piperidine-1,4-dicarboxylate Methyl1-(tert-Butoxycbonyl)-4-piperidinecboxylate> 1-tert-Butyl 4-methyl 1,4-piperidinedicboxylate tert-Butyl Methyl piperidine-1,6-dicboxylate tert-Butyl Methyl piperidine-1,7-dicboxylate 1-TERT-BUTYL 4-METHYL PIPERIDINE-1,4-DICBOXYLATE tert-Butyl Methyl piperidine-1,8-dicboxylate 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic Acid Methyl Ester 1-N-Boc-4-Piperidinecarboxylic acid methyl ester N-BOC-4-PIPERIDINECBOXYLIC ACID METHYL ESTER tert-Butyl Methyl piperidine-1,9-dicboxylate tert-Butyl methyl piperidine-1,4-dicboxylate |
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 307.4±35.0 °C at 760 mmHg |
| Melting Point | 35 °C |
| Molecular Formula | C12H21NO4 |
| Molecular Weight | 243.299 |
| Flash Point | 139.7±25.9 °C |
| Exact Mass | 243.147064 |
| PSA | 55.84000 |
| LogP | 1.51 |
| Vapour Pressure | 0.0±0.7 mmHg at 25°C |
| Index of Refraction | 1.473 |
| Hazard Codes | Xi |
|---|---|
| HS Code | 2933399090 |
|
~87%
124443-68-1 |
| Literature: AXYS PHARMACEUTICALS, INC. Patent: WO2006/86609 A2, 2006 ; Location in patent: Page/Page column 160 ; WO 2006/086609 A2 |
|
~95%
124443-68-1 |
| Literature: Baindur, Nand; Gaul, Michael David; Kreutter, Kevin Douglas; Baumann, Christian Andrew; Kim, Alexander J.; Xu, Guozhang; Tuman, Robert W.; Johnson, Dana L. Patent: US2006/281772 A1, 2006 ; Location in patent: Page/Page column 51 ; US 20060281772 A1 |
|
~99%
124443-68-1 |
| Literature: Renslo, Adam R.; Atuegbu, Andy; Herradura, Prudencio; Jaishankar, Priyadarshini; Ji, Mingzhe; Leach, Karen L.; Huband, Michael D.; Dermyer, Michael R.; Wu, Luping; Vara Prasad; Gordeev, Mikhail F. Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 18 p. 5036 - 5040 |
|
~92%
124443-68-1 |
| Literature: Sandanayaka, Vincent P.; Zask, Arie; Venkatesan, Aranapakam M.; Baker, Jannie Tetrahedron Letters, 2001 , vol. 42, # 28 p. 4605 - 4607 |
|
~%
124443-68-1 |
| Literature: US5891889 A1, ; US 5891889 A |
|
~91%
124443-68-1 |
| Literature: Carr, Albert A.; Hay, David A.; Kane, John M.; Staeger, Michael A. Journal of Organic Chemistry, 1990 , vol. 55, # 4 p. 1399 - 1401 |
|
~99%
124443-68-1 |
| Literature: Wu, Chengde; Anderson, C. Eric; Bui, Huong; Dupre, Brian; Gao, Daxin; Holland, George W.; Kassir, Jamal; Li, Wen; Wang, Junmei Patent: US2005/54850 A1, 2005 ; |
| Precursor 10 | |
|---|---|
| DownStream 10 | |
| HS Code | 2933399090 |
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |