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135544-68-2

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135544-68-2 Usage

Chemical Properties

Low melting solid to liquid

Uses

N-(Allyloxycarbonyloxy)succinimide (alloc-Su) can be used as: A building block for the preparation of glycopeptide scaffolds. A reagent in the synthesis of various functional cyclic carbonate monomers from 2-amino-1,3-propane diols.

Check Digit Verification of cas no

The CAS Registry Mumber 135544-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,4 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135544-68:
(8*1)+(7*3)+(6*5)+(5*5)+(4*4)+(3*4)+(2*6)+(1*8)=132
132 % 10 = 2
So 135544-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO5/c1-2-5-13-8(12)14-9-6(10)3-4-7(9)11/h2H,1,3-5H2

135544-68-2 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • TCI America

  • (A2302)  N-(Allyloxycarbonyloxy)succinimide  >97.0%(GC)

  • 135544-68-2

  • 5g

  • 720.00CNY

  • Detail
  • TCI America

  • (A2302)  N-(Allyloxycarbonyloxy)succinimide  >97.0%(GC)

  • 135544-68-2

  • 25g

  • 2,550.00CNY

  • Detail
  • Aldrich

  • (738158)  N-(Allyloxycarbonyloxy)succinimide  96%

  • 135544-68-2

  • 738158-5G

  • 687.96CNY

  • Detail
  • Aldrich

  • (738158)  N-(Allyloxycarbonyloxy)succinimide  96%

  • 135544-68-2

  • 738158-25G

  • 2,701.53CNY

  • Detail

135544-68-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dioxopyrrolidin-1-yl) prop-2-enyl carbonate

1.2 Other means of identification

Product number -
Other names AmbotzRL-1108

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:135544-68-2 SDS

135544-68-2Relevant articles and documents

Terminal Alkenes as Versatile Chemical Reporter Groups for Metabolic Oligosaccharide Engineering

Sp?te, Anne-Katrin,Schart, Verena F.,Sch?llkopf, Sophie,Niederwieser, Andrea,Wittmann, Valentin

, p. 16502 - 16508 (2014)

The Diels-Alder reaction with inverse electron demand (DAinv reaction) of 1,2,4,5-tetrazines with electron rich or strained alkenes was proven to be a bioorthogonal ligation reaction that proceeds fast and with high yields. An important application of the DAinv reaction is metabolic oligosaccharide engineering (MOE) which allows the visualization of glycoconjugates in living cells. In this approach, a sugar derivative bearing a chemical reporter group is metabolically incorporated into cellular glycoconjugates and subsequently derivatized with a probe by means of a bioorthogonal ligation reaction. Here, we investigated a series of new mannosamine and glucosamine derivatives with carbamate-linked side chains of varying length terminated by alkene groups and their suitability for labeling cell-surface glycans. Kinetic investigations showed that the reactivity of the alkenes in DAinv reactions increases with growing chain length. When applied to MOE, one of the compounds, peracetylated N-butenyloxycarbonylmannosamine, was especially well suited for labeling cell-surface glycans. Obviously, the length of its side chain represents the optimal balance between incorporation efficiency and speed of the labeling reaction. Sialidase treatment of the cells before the bioorthogonal labeling reaction showed that this sugar derivative is attached to the glycans in form of the corresponding sialic acid derivative and not epimerized to another hexosamine derivative to a considerable extent. Shine bright: Metabolic oligosaccharide engineering with peracetylated N-butenyloxycarbonylmannosamine 1 (n=2) leads to cell-surface glycoconjugate staining with higher intensity compared with previously reported terminal alkene reporters. Analogues with shorter (n=1) or longer (n=3-4) side chains are much less efficient for labeling.

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