ChemicalBook > CAS DataBase List > N-T-BOC-PYRROLE

N-T-BOC-PYRROLE

Product Name
N-T-BOC-PYRROLE
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
Formula Weight
167.21
MOL File
5176-27-2.mol
More
Less

N-T-BOC-PYRROLE Property

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
InChI
InChI=1S/C9H13NO2/c1-9(2,3)12-8(11)10-6-4-5-7-10/h4-7H,1-3H3
InChIKey
IZPYBIJFRFWRPR-UHFFFAOYSA-N
SMILES
N1(C(OC(C)(C)C)=O)C=CC=C1
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
2933998090
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
425834
Product name
N-Boc-pyrrole
Purity
98%
Packaging
25ml
Price
$67.2
Updated
2025/07/31
Sigma-Aldrich
Product number
425834
Product name
N-Boc-pyrrole
Purity
98%
Packaging
100ml
Price
$237
Updated
2025/07/31
TRC
Product number
P997900
Product name
Pyrrole-1-carboxylicAcidtert-ButylEster
Packaging
10g
Price
$115
Updated
2021/12/16
AK Scientific
Product number
J97221
Product name
N-Boc-pyrrole
Packaging
1g
Price
$10
Updated
2021/12/16
Matrix Scientific
Product number
150363
Product name
tert-Butyl 1H-pyrrole-1-carboxylate
Purity
95%
Packaging
25g
Price
$33
Updated
2021/12/16
More
Less

N-T-BOC-PYRROLE Chemical Properties,Usage,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.

Uses

N-Boc-pyrrole was used in the synthesis of 1-(tert-butoxycarbonyl)-1H-pyrrol-2-ylboronic acid by treating with n-BuLi and subsequent reaction with trimethyl borate.
It may be used as starting material in the synthesis of the following:

  • tropane drivatives
  • N-boc-2-(4-methoxyphenyl)pyrrole
  • N-boc-pyrrol-2-ylboronic acid

Synthesis Reference(s)

The Journal of Organic Chemistry, 31, p. 764, 1966 DOI: 10.1021/jo01341a027

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.

Synthesis

109-97-7

24424-99-5

5176-27-2

General procedure for the synthesis of tert-butyl 1-pyrrolecarboxylate from pyrrole and di-tert-butyl dicarbonate: di-tert-butyl dicarbonate (Boc2O, 9.8 g, 44.7 mmol) and triethylamine (TEA, 6.3 mL, 44.7 mmol) were added sequentially to a solution of pyrrole (3.0 g, 29.8 mmol) in dichloromethane (DCM, 15 mL). The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, extraction was performed with dichloromethane (2 x 400 mL) and water (400 mL). The organic layers were combined, dried over anhydrous magnesium sulfate (MgSO4) and concentrated under reduced pressure to afford tert-butyl 1-pyrrolecarboxylate (26) as a white solid (7.5 g). Yield: 94%; 1H NMR (300 MHz, CDCl3) δ (ppm): 7.26 (s, 2H), 7.24 (t, J=2.4 Hz, 1H), 6.22 (t, J=2.4 Hz, 1H), 1.60 (d, J=11.7 Hz, 9H); ESI-MS [M+H]+=169.0.

References

[1] European Journal of Organic Chemistry, 2005, # 11, p. 2207 - 2212
[2] Angewandte Chemie - International Edition, 2015, vol. 54, # 52, p. 15739 - 15743
[3] Angew. Chem., 2015, vol. 127, # 52, p. 15965 - 15969,5
[4] European Journal of Medicinal Chemistry, 2011, vol. 46, # 4, p. 1153 - 1164
[5] Medicinal Chemistry, 2018, vol. 14, # 5, p. 485 - 494

N-T-BOC-PYRROLE Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

N-T-BOC-PYRROLE Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
Accela ChemBio Inc.
Tel
+1-858-6993322
Fax
(+1)-858-876-1948
Email
info@accelachem.com
Country
United States
ProdList
21193
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Synthonix Inc
Tel
--
Fax
--
Email
info@synthonix.com
Country
United States
ProdList
6872
Advantage
58
Alfa Chemistry
Tel
--
Fax
--
Email
info@Alfa-Chemistry.com
Country
United States
ProdList
6814
Advantage
0
Best PharmaTech, Inc.
Tel
--
Fax
--
Email
info@bestpharmatech.com
Country
United States
ProdList
867
Advantage
50
Sarchem Laboratories, Inc.
Tel
--
Fax
--
Email
sarchem@aol.com
Country
United States
ProdList
198
Advantage
50
Sarchem Laboratories, Inc.
Tel
--
Fax
--
Email
info@sarchemlabs.com
Country
United States
ProdList
736
Advantage
58
Combi-Blocks, Inc.
Tel
--
Fax
--
Email
les@combi-blocks.com
Country
United States
ProdList
2555
Advantage
58
Crescent Chemical Company
Tel
--
Fax
--
Email
fran@creschem.com
Country
United States
ProdList
1441
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
MilliporeSigma (Sigma-Aldrich Corp.)
Tel
--
Fax
--
Email
@sial.com
Country
United States
ProdList
5414
Advantage
58
Bridge Organics Company
Tel
--
Fax
--
Email
businessoffice@bridgeorganics.com
Country
United States
ProdList
85
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Kingston Chemistry
Tel
--
Fax
--
Email
contact@kingstonchem.com
Country
United States
ProdList
448
Advantage
60
Reagent World
Tel
--
Fax
--
Email
Sales@ReagentWorld.com
Country
United States
ProdList
1637
Advantage
50
Amfinecom Inc.
Tel
--
Fax
--
Email
sales@amfinecom.com
Country
United States
ProdList
3062
Advantage
50
Interchem Corporation
Tel
--
Fax
--
Email
fc@interchem.com
Country
United States
ProdList
38
Advantage
60
Anvia Chemicals, LLC
Tel
--
Fax
--
Email
sales@anviachem.com
Country
United States
ProdList
3933
Advantage
0
AOBChem USA
Tel
--
Fax
--
Email
sales@aobchem.com
Country
United States
ProdList
3487
Advantage
50
Combi-Blocks Inc.
Tel
--
Fax
--
Email
sales@combi-blocks.com
Country
United States
ProdList
6618
Advantage
69
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
More
Less

View Lastest Price from N-T-BOC-PYRROLE manufacturers

Career Henan Chemical Co
Product
N-T-BOC-PYRROLE 5176-27-2
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
JD 832
Release date
2019-09-02

5176-27-2, N-T-BOC-PYRROLERelated Search:


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