CasNo.1126-09-6,CAS:1126-09-6 C8H15NO2 Ethyl 4-piperidinecarboxylate,(1126-09-6) Suppliers

500 Gram	Negotiable

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Purity: 99%
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CAS:1126-09-6 C8H15NO2 Ethyl 4-piperidinecarboxylate CAS:1126-09-6 C8H15NO2 factory price high purity 99% CAS:1126-09-6 C8H15NO2 technical grade or OLED grade

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Appearance:white poweder
Application:CAS:1126-09-6 C8H15NO2 technical grade or OLED grade
PackAge:Plastic vacuum packaging bag or bucket
ProductionCapacity:1|Metric Ton|Day
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Ethyl 4-piperidinecarboxylate Basic information

Product Name:	Ethyl 4-piperidinecarboxylate
Synonyms:	4-Carbethoxypiperidine;ISONIPECOTINIC ACID ETHYL ESTER;ISONIPECOTIC ACID ETHYL ESTER;ETHYL ISONIPECOTATE;ETHYL PIPERIDINE-4-CARBOXYLATE;ETHYL 4-PIPERIDINECARBOXYLATE;LABOTEST-BB LT00159543;4-PIPERDINECARBOXYLIC ACID, ETHYL ESTER
CAS:	1126-09-6
MF:	C8H15NO2
MW:	157.21
EINECS:	214-416-7
Product Categories:	Pharmaceutical Intermediates;Piperidines, Piperidones, Piperazines;pharmacetical;AMINOACIDS DERIVATIVES;Piperidine;Building Blocks;C8;Chemical Synthesis;Heterocyclic Building Blocks;Piperidines;Heterocycles
Mol File:	1126-09-6.mol

Ethyl 4-piperidinecarboxylate Chemical Properties

bp	204 °C(lit.)
density	1.02 g/mL at 25 °C(lit.)
refractive index	n20/D 1.459(lit.)
Fp	176 °F
Water Solubility	miscible
BRN	118419
CAS DataBase Reference	1126-09-6(CAS DataBase Reference)
NIST Chemistry Reference	Ethyl piperidine-4-carboxylate(1126-09-6)

Safety Information

Hazard Codes	C,Xi
Risk Statements	34-36/37/38
Safety Statements	23-24/25-36-26
WGK Germany	3
Hazard Note	Irritant
HS Code	29333999

MSDS Information

Provider	Language
Ethyl 4-piperidinecarboxylate	English
SigmaAldrich	English
ACROS	English
ALFA	English

Ethyl 4-piperidinecarboxylate Usage And Synthesis

Chemical Properties	clear colorless to slightly brown liquid
Usage	Reactant for synthesis of:• ;SMN protein modulators1• ;β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition2• ;Nitroethylenediamines by nucleophilic ring opening of nitroimidazolidinone3• ;RhoA inhibitors for cardiovascular disease therapy4• ;Saccharin derived Mannich bases as antimicrobials and antioxidants5Reactant for one-pot reductive amination and Suzuki-Miyaura cross coupling of formyl aryl and heteroaryl MIDA boronates6
Usage	Reactant for synthesis of SMN protein modulators and β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition.

Ethyl 4-piperidinecarboxylate Preparation Products And Raw materials

Preparation Products

(S)-3-Aminoquinuclidine dihydrochloride-->1-(2,6-DIMETHOXYBENZYL)PIPERIDIN-4-AMINE HYDROCHLORIDE-->3-Aminoquinuclidine dihydrochloride-->Ethyl N-Boc-4-methylpiperidine-4-carboxylate-->(R)-(-)-3-Quinuclidinol -->(R)-3-Aminoquinuclidine dihydrochloride-->3-Quinuclidinone hydrochloride-->1-BOC-4-ETHYL-4-PIPERIDINECARBOXYLIC ACID-->1-Boc-4-methylpiperidine-4-carboxylic acid-->Ethyl 2-(4-(ethoxycarbonyl)piperidin-1-yl)pyrimidine-5-carboxylate-->(R)-3-Quinuclidinol hydrochloride-->Ethyl 2-(4-(ethoxycarbonyl)piperidin-1-yl)-6-(trifluoromethyl)pyrimidine-4-carboxylate-->(S)-(+)-3-Quinuclidinol-->quinuclidine-3-carboxylic acid -->1-(PYRIMIDIN-2-YL)PIPERIDINE-3-CARBOHYDRAZIDE-->1-(PYRIMIDIN-2-YL)PIPERIDINE-4-CARBOXYLIC ACID HYDROCHLORIDE-->4-ALLYL-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER-->ETHYL 1-(2-CHLOROACETYL)-4-PIPERIDINECARBOXYLATE

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