Ethyl N-Boc-4-methylpiperidine-4-carboxylate structure
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Common Name | Ethyl N-Boc-4-methylpiperidine-4-carboxylate | ||
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CAS Number | 189442-87-3 | Molecular Weight | 271.35300 | |
Density | 1.0134 | Boiling Point | 329.7ºC at 760mmHg | |
Molecular Formula | C14H25NO4 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 110ºC | |
Symbol |
GHS05, GHS06 |
Signal Word | Danger |
Name | 1-O-tert-butyl 4-O-ethyl 4-methylpiperidine-1,4-dicarboxylate |
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Synonym | More Synonyms |
Density | 1.0134 |
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Boiling Point | 329.7ºC at 760mmHg |
Molecular Formula | C14H25NO4 |
Molecular Weight | 271.35300 |
Flash Point | 110ºC |
Exact Mass | 271.17800 |
PSA | 55.84000 |
LogP | 2.52620 |
Vapour Pressure | 0.000175mmHg at 25°C |
Index of Refraction | 1.4554 |
Symbol |
GHS05, GHS06 |
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Signal Word | Danger |
Hazard Statements | H301-H315-H318-H335 |
Precautionary Statements | P261-P280-P301 + P310-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | T: Toxic; |
Risk Phrases | R25;R37/38;R41 |
Safety Phrases | 26-36/37/39-45 |
RIDADR | UN 2810 |
Hazard Class | 6.1 |
HS Code | 2933399090 |
~99% Ethyl N-Boc-4-m... CAS#:189442-87-3 |
Literature: ARRAY BIOPHARMA INC. Patent: WO2008/121687 A2, 2008 ; Location in patent: Page/Page column 43; 89; 94 ; WO 2008/121687 A2 |
~% Ethyl N-Boc-4-m... CAS#:189442-87-3 |
Literature: WO2005/30209 A1, ; Page/Page column 46 ; WO 2005/030209 A1 |
Precursor 2 | |
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DownStream 8 | |
HS Code | 2933399090 |
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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% |
Facile synthesis of 4-substituted-4-aminopiperidine derivatives, the key building block of piperazine-based CCR5 antagonists.
Bioorg. Med. Chem. Lett. 14 , 3675, (2004) 4-Substituted-4-aminopiperidine is an interesting structural motif found in a number of bioactive compounds. An efficient and convenient method for the synthesis of 4-differently substituted-4-aminopi... |
1-BOC-4-METHYL-ISONIPECOTIC ACID ETHYL ESTER |
N-tert-butoxycarbonyl-4-methylisonipecotic acid ethyl ester |
4-methyl-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethvl ester |
1-tert-Butyl 4-ethyl 4-methylpiperidine-1,4-dicarboxylate |
Ethyl N-Boc-4-methylpiperidine-4-carboxylate |
1-BOC-4-METHYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL ESTER |
Ethyl N-Boc-4-Methylpiperidine-4-Carboxylate |
4-methyl piperidine-1,4-dicarboxylic acid-1-tert-butylester 4-ethyl ester |
4-Methyl-1,4-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 4-ethyl ester |
Ethyl 1-N-Boc-4-methyl-piperidine-carboxylate |
ethyl N-t-butoxycarbonyl-4-methylpiperidine-4-carboxylate |
O1-tert-butyl O4-ethyl 4-methylpiperidine-1,4-dicarboxylate |
1-tert-butyl 4-ethyl 4-methylpiperidine-1,4-dicarboxylate |
1-tert-Butoxycarbonyl-4-methylpiperidine-4-carboxylic acid ethyl ester |