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N-BOC-2-MALEIMIDOETHYLAMINE

Product Name
N-BOC-2-MALEIMIDOETHYLAMINE
CAS No.
134272-63-2
Chemical Name
N-BOC-2-MALEIMIDOETHYLAMINE
Synonyms
Mal-Boc;BocNH-Mal;Mal-NH-Boc;N-BOC-2-MaleMidoethylaMine;N-BOC-2-MALEIMIDOETHYLAMINE;N-(2-Boc-aMino)ethyl MaleiMide;N-Boc-2-maleimidoethylamine 98%;N-(2-tert-butyloxycarbonylamino)ethylmaleimide;tert-butyl N-[2-(2,5-dioxopyrrol-1-yl)ethyl]carbamate;tert-butyl 2-(2,5-dioxo-2H-pyrrol-1(5H)-yl)ethylcarbamate
CBNumber
CB11519492
Molecular Formula
C11H16N2O4
Formula Weight
240.26
MOL File
134272-63-2.mol
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N-BOC-2-MALEIMIDOETHYLAMINE Property

Melting point:
110-115°C
Boiling point:
390.9±25.0 °C(Predicted)
Density 
1.210±0.06 g/cm3(Predicted)
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Solid
pka
12.09±0.46(Predicted)
color 
White to Pale Pink
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

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

Biosynth Carbosynth
Product number
FB18914
Product name
N-(2-Boc-amino)ethyl maleimide
Packaging
500mg
Price
$200
Updated
2021/12/16
SynQuest Laboratories
Product number
4H48-1-MP
Product name
tert-Butyl N-[2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl]carbamate
Packaging
500mg
Price
$208
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18914
Product name
N-(2-Boc-amino)ethyl maleimide
Packaging
1g
Price
$260
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18914
Product name
N-(2-Boc-amino)ethyl maleimide
Packaging
250mg
Price
$120
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB18914
Product name
N-(2-Boc-amino)ethyl maleimide
Packaging
2g
Price
$500
Updated
2021/12/16
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N-BOC-2-MALEIMIDOETHYLAMINE Chemical Properties,Usage,Production

Description

tert-butyl 2-(2,5-dioxo-2H-pyrrol-1(5H)-yl)ethylcarbamate contains a maleimide group and a Boc-protected amine group. The protected amine can be deprotected under acidic conditions. The maleimide group will react with a thiol group to form a covalent bond, enabling the connection of biomolecule with a thiol.

Chemical Properties

White Crystalline Solid

Uses

N-BOC-2-MALEIMIDOETHYLAMINE is used in the Mitsunobu reaction: a novel method for the synthesis of bifunctional maleimide linkers.

N-BOC-2-MALEIMIDOETHYLAMINE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-BOC-2-MALEIMIDOETHYLAMINE Suppliers

Canada 1 China 71 India 2 United Kingdom 2 United States 5 Global 81
A.J Chemicals
Tel
--
Fax
--
Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58
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View Lastest Price from N-BOC-2-MALEIMIDOETHYLAMINE manufacturers

Career Henan Chemical Co
Product
N-BOC-2-MALEIMIDOETHYLAMINE 134272-63-2
Price
US $3.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
200KG
Release date
2020-02-20

134272-63-2, N-BOC-2-MALEIMIDOETHYLAMINERelated Search:

Maleimide N-BOC-2-MALEIMIDOETHYLAMINE

  • N-BOC-2-MALEIMIDOETHYLAMINE
  • N-(2-Boc-aMino)ethyl MaleiMide
  • tert-Butyl N-[2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl]carbamate
  • tert-butyl 2-(2,5-dioxo-2H-pyrrol-1(5H)-yl)ethylcarbamate
  • N-(2-tert-butyloxycarbonylamino)ethylmaleimide
  • N-Boc-2-maleimidoethylamine 98%
  • N-[2-(2,5-Dihydro-2,5-dioxo-1H-pyrrol-1-yl)ethyl]carbaMic Acid 1,1-DiMethylethyl Ester
  • [2-(2,5-Dioxo-2,5-dihydro-pyrrol-1-yl)-ethyl]-carbaMic acid tert-butyl ester
  • tert-Butyl (2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)carbaMate
  • N-BOC-2-MaleMidoethylaMine
  • Mal-NH-Boc
  • Carbamic acid, N-[2-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)ethyl]-, 1,1-dimethylethyl ester
  • BocNH-Mal
  • Mal-Boc
  • tert-butyl N-[2-(2,5-dioxopyrrol-1-yl)ethyl]carbamate
  • 134272-63-2
  • Maleimide Derivatives, MTS & Sulfhydryl Active Reagents
  • Cross Linking Reagents
  • Maleimide Derivatives
  • MTS & Sulfhydryl Active Reagents