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N-BOC-IMIDAZOLE

Product Name
N-BOC-IMIDAZOLE
CAS No.
49761-82-2
Chemical Name
N-BOC-IMIDAZOLE
Synonyms
tert-Butyl 1H-imidazole-1-carboxylate;N-TERT-BUTOXYCARBONYLIMIDAZOLE;BOC-IMIDAZOLE;N-BOC-IMIDAZOLE;N-T-BOC-IMIDAZOLE;N-Boc-imidazole,98%;1-Boc-imidazole, 98%;Medetomidine Impurity 58;N-tert-Butoxycarbonylimidazo;N-Boc-imidazole≥ 98%(Titration)
CBNumber
CB6328955
Molecular Formula
C8H12N2O2
Formula Weight
168.19
MOL File
49761-82-2.mol
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N-BOC-IMIDAZOLE Property

Melting point:
45-47 °C(lit.)
Boiling point:
147-150 °C(lit.)
Density 
1.1835 (rough estimate)
refractive index 
1.4200 (estimate)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Soluble in hexane, acetone, and DMF.
form 
powder to crystal
pka
3.49±0.10(Predicted)
color 
White to Almost white
Sensitive 
Moisture Sensitive
BRN 
607792
InChI
InChI=1S/C8H12N2O2/c1-8(2,3)12-7(11)10-5-4-9-6-10/h4-6H,1-3H3
InChIKey
MTBKGWHHOBJMHJ-UHFFFAOYSA-N
SMILES
C1N(C(OC(C)(C)C)=O)C=CN=1
CAS DataBase Reference
49761-82-2(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933299090
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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.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
424013
Product name
1-(tert-Butoxycarbonyl)imidazole
Purity
97%
Packaging
10g
Price
$81.1
Updated
2022/05/15
TCI Chemical
Product number
B0916
Product name
N-tert-Butoxycarbonylimidazole
Purity
>98.0%(T)
Packaging
10g
Price
$63
Updated
2024/03/01
Alfa Aesar
Product number
L00506
Product name
1-Boc-imidazole, 98%
Packaging
5g
Price
$26.65
Updated
2024/03/01
Alfa Aesar
Product number
L00506
Product name
1-Boc-imidazole, 98%
Packaging
25g
Price
$68.65
Updated
2024/03/01
TRC
Product number
B656725
Product name
N-Boc-Imidazole
Packaging
10mg
Price
$45
Updated
2021/12/16
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N-BOC-IMIDAZOLE Chemical Properties,Usage,Production

Chemical Properties

White powder

Uses

1-Boc-imidazole is used in the preparation of water soluble polyrotaxane, via modification of α-cyclodextrin in the presence of KOH and N,N?-carbonyldiimidazole.

General Description

1-(tert-butoxycarbonyl)imidazole is an imidazole derivative. Its gas-phase elimination kinetics study has been studied both theoretically and experimentally.

N-BOC-IMIDAZOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-BOC-IMIDAZOLE Suppliers

Americas 1 China 135 Europe 1 Germany 2 India 6 Japan 1 Switzerland 1 United Kingdom 4 United States 16 Global 167
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71
ABCR GmbH & CO. KG
Tel
--
Fax
--
Email
info@abcr.de
Country
Germany
ProdList
6831
Advantage
75
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View Lastest Price from N-BOC-IMIDAZOLE manufacturers

Career Henan Chemical Co
Product
N-BOC-IMIDAZOLE 49761-82-2
Price
US $1.00/KG
Min. Order
1KG
Purity
>98%
Supply Ability
200kg
Release date
2019-08-30

49761-82-2, N-BOC-IMIDAZOLERelated Search:

FMOC-HIS(BOC)-OH N-BOC-IMIDAZOLE N,N'-Di-tert-butoxycarbonyl-L-histidine 7-(tert-butoxycarbonyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine-2-carboxylic acid FMOC-HIS(BOC)-OPFP BOC-D-HIS(BOC)-OH FMOC-L-HIS(BOC)-OH DCHA FMOC-D-HIS(BOC)-OH FMOC-D-HIS(BOC)-OPFP 5-AMINO-1-BOC-BENZOIMIDAZOLE FMOC-D-HIS(BOC)-OH CHA 2-HYDROXY-BENZOIMIDAZOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER BOC-D-HIS(BOC)-OH BENZENE Boc-His(1-Boc)-OSu N-Boc HistaMine N(ALPHA) N-(IM)-DI-BOC-L-HISTIDINE FMOC-HIS(BOC)-OL SPECS AI-942/42301869

  • 1H-Imidazole-1-carboxylic acid, 1,1-dimethylethyl ester
  • tert-Butyl 1H-imidazole-1-carboxylate
  • BOC-IMIDAZOLE
  • N-Boc-imidazole,98%
  • 1-(TERT-BUTOXYCARBONYL)IMIDAZOLE
  • N-BOC-IMIDAZOLE
  • N-T-BOC-IMIDAZOLE
  • N-TERT-BUTOXYCARBONYLIMIDAZOLE
  • 1-Boc-imidazole, 98%
  • 1,1-Dimethylethyl 1H-imidazole-1-carboxylate
  • tert-Butyl imidazole-1-carboxylate
  • 1-(tert-Butoxycarbonyl)iMidazole, 98%+
  • 1-(tert-Butoxycarbonyl)imidazole 97%
  • N-Boc-imidazole≥ 98%(Titration)
  • Imidazole-1-carboxylic acid tert-butyl ester
  • 1-imidazolecarboxylic acid tert-butyl ester
  • 1-(Tert-butoxycarbonyl)imidazole, 98%, for synthesis
  • N-tert-Butoxycarbonylimidazole &gt
  • Medetomidine Impurity 58
  • N-tert-Butoxycarbonylimidazo
  • 49761-82-2 C8H12N2O2 N-BOC-IMIDAZOLE
  • 49761-82-2
  • 49861-82-2
  • Building Blocks
  • Imidazoles
  • Heterocyclic Building Blocks
  • Protection & Derivatization Reagents (for Synthesis)
  • Protective Reagents (Peptide Synthesis)
  • Peptide Synthesis
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Protective Reagents (Peptide Synthesis)
  • Biochemistry
  • Peptide Synthesis
  • Synthetic Organic Chemistry
  • Building Blocks
  • Heterocyclic Building Blocks
  • Imidazoles
  • Protection & Derivatization Reagents (for Synthesis)