N-T-BOC-PYRROLE

N-T-BOC-PYRROLE Structure
CAS No.
5176-27-2
Chemical Name:
N-T-BOC-PYRROLE
Synonyms
tert-butyl 1H-pyrrole-1-carboxylate;N-Boc-Pyrrole;e-1-CarboxyL;1-Boc-pyrrole;ate(WX690266);N-T-BOC-PYRROLE;N-BOC-1H-PYRROLE;N-T-BOC-PYRROLE-1;N-Boc-pyrrole 98%;N-Boc-pyrrole
CBNumber:
CB4315199
Molecular Formula:
C9H13NO2
Molecular Weight:
167.21
MOL File:
5176-27-2.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

N-T-BOC-PYRROLE Properties

Boiling point 91-92 °C20 mm Hg(lit.)
Density 1 g/mL at 25 °C(lit.)
refractive index n20/D 1.4685(lit.)
Flash point 167 °F
storage temp. Sealed in dry,Room Temperature
solubility Acetonitrile, Dichloromethane, Ethyl Acetate, Methanol, Tetrahydrofuran
form Solution
pka -6.10±0.70(Predicted)
color Colorless to yellow
InChIKey IZPYBIJFRFWRPR-UHFFFAOYSA-N

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26
WGK Germany  3
HS Code  2933998090

N-T-BOC-PYRROLE price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 425834 N-Boc-pyrrole 98% 5176-27-2 25ML ₹6635.73 2022-06-14 Buy
Sigma-Aldrich(India) 425834 N-Boc-pyrrole 98% 5176-27-2 100ML ₹19744.8 2022-06-14 Buy
Product number Packaging Price Buy
425834 25ML ₹6635.73 Buy
425834 100ML ₹19744.8 Buy

N-T-BOC-PYRROLE Chemical Properties,Uses,Production

Chemical Properties

Colorless liquid

Uses

Pyrrole-1-carboxylic Acid tert-Butyl Ester is an intermediate in the synthesis of pyrrole derived anti-cancer Agent.

General Description

N-Boc-pyrrole is an N-protected pyrrole. It undergoes Diels–Alder reaction with enantiomerically pure allene-1,3-dicarboxylates to form endo-adducts with retention in configurations at two newly generated stereogenic centers. It also undergoes cyclopropanation with methyl phenyldiazoacetate to form both monocyclopropane and dicyclopropane. Its Ir-catalyzed C-H borylation followed by cross coupling with 3-chlorothiophene to form biheterocycle has been reported.

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TERT-BUTYL PYRROL-1-CARBOXYLATE TERT-BUTYL 1-PYRROLECARBOXYLATE N-T-BOC-PYRROLE N-BOC-1H-PYRROLE tert-butyl-pyrrole-carboxylate 1-Boc-pyrrole t-Butyl 1H-pyrrole-1-carboxylate tert-butyl-pyrrole-carboxylate,98% N-Boc-pyrrole,tert-Butyl 1-pyrrolecarboxylate 1H-Pyrrole-1-carboxylic acid, 1,1-diMethylethyl ester N-T-BOC-PYRROLE-1 Pyrrole-1-carboxylic Acid tert-Butyl Ester N-Boc-pyrrole 98% tert-Butylpyrrole-1-carboxylate N-(t-Butoxycarbonyl)pyrrole N-tert-Butoxycarbonyl-1H-pyrrole N-(tert-butyloxycarbonyl)pyrrole N-Boc-pyrrole Tert-Butyl 1H-Pyrrole-1-Carboxylate(WX690266) 1-pyrrolecarboxylic acid tert-butyl ester N-tert-Butoxycarbonyl-1H-pyrrol N-Boc-pyrrole, 97%, for synthesis ate(WX690266) e-1-CarboxyL tert-butyl 1H-pyrrole-1-carboxylate N-Boc-Pyrrole 1-(tert-Butoxycarbonyl)pyrrole 5176-27-2 Building Blocks Heterocyclic Building Blocks Pyrroles carboxylic ester Building Blocks Chemical Synthesis Heterocyclic Building Blocks Pyrroles