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Key Documents

Safety Information

341096

Sigma-Aldrich

Succinimidyl 2,2,2-trichloroethyl carbonate

98%

Synonym(s):

N-(2,2,2-Trichloroethoxycarbonyloxy)succinimide

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About This Item

Empirical Formula (Hill Notation):
C7H6Cl3NO5
CAS Number:
Molecular Weight:
290.49
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

mp

111-113 °C (lit.)

storage temp.

2-8°C

SMILES string

ClC(Cl)(Cl)COC(=O)ON1C(=O)CCC1=O

InChI

1S/C7H6Cl3NO5/c8-7(9,10)3-15-6(14)16-11-4(12)1-2-5(11)13/h1-3H2

InChI key

WBZXNGAFYBGQFE-UHFFFAOYSA-N

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Application

Succinimidyl 2,2,2-trichloroethyl carbonate was used in the synthesis of:
  • methyl [phenyl 5-(2,2,2-trichloroethoxycarbonylamino)-3,5-dideoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid]-onate[1]
  • phenyl 3,4-di-O-benzyl-6-O-(tert-butyl-dimethyl-silyl)-1-selanyl-2-(2,2,2-trichloroethoxycarbonylamine)-β-D-galactopyranoside[2]

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

341096-VAR:
341096-BULK:
341096-10G:
341096-50G:


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Chien-Tai Ren et al.
The Journal of organic chemistry, 72(14), 5427-5430 (2007-06-21)
Synthesis of a tetrasaccharide glycosyl glycerol, the core structure of glycoglycerolipid from Meiothermus taiwanensis ATCC BAA-400, was described. A one-pot glycosylation with three components was employed as a key step.
Chien-Tai Ren et al.
The Journal of organic chemistry, 67(4), 1376-1379 (2002-02-16)
The preparation of a disaccharide 2, Neu5Ac-alpha-(2-->5)Neu5Gc having a alpha-benzyl protecting group at the reducing end, by the coupling of the easily accessible building units 4 and 5 is described. Subsequent deprotection of the coupling adduct led to the isolation

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