Skip to Content
Merck
CN

Key Documents

View All Documentation

738158

N-(Allyloxycarbonyloxy)succinimide

96%, liquid

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C8H9NO5
CAS Number:
135544-68-2
Molecular Weight:
199.16
UNSPSC Code:
12352005
PubChem Substance ID:
329765253
NACRES:
NA.22
MDL number:
MFCD02684388
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

N-(Allyloxycarbonyloxy)succinimide, 96%

Quality Level

100

assay

96%

form

liquid

refractive index

n20/D 1.482

density

1.287 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

C=CCOC(=O)ON1C(=O)CCC1=O

InChI

1S/C8H9NO5/c1-2-5-13-8(12)14-9-6(10)3-4-7(9)11/h2H,1,3-5H2

InChI key

OIXALTPBNZNFLJ-UHFFFAOYSA-N

Application

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

242.6 °F

flash_point_c

117 °C

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKDB2877
MKCW9498
MKCS5448
MKCR6908
MKCR6909

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and in vitro evaluation of bisphosphonated glycopeptide prodrugs for the treatment of osteomyelitis
Tanaka KSE, et al.
Bioorganic & medicinal chemistry letters, 20(4), 1355-1359 (2010)
2-Amino-1, 3-propane diols: a versatile platform for the synthesis of aliphatic cyclic carbonate monomers
Venkataraman S, et al.
Polym. Chem., 4(10), 2945-2948 (2013)
Bo Wu et al.
Molecules (Basel, Switzerland), 25(19) (2020-10-07)
Four bis-lactam [i, i+4]-stapled peptides with d- or l-α-methyl-thialysines were constructed on a model peptide sequence derived from p110α[E545K] and subjected to circular dichroism (CD) and proteolytic stability assessment, alongside the corresponding bis-lactam [i, i+4]-stapled peptide with l-thialysine. The %

Global Trade Item Number

SKUGTIN
738158-5G04061833555552
738158-25G04061833510599