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CAS RN: 74124-79-1 | Product Number: D1662

Di(N-succinimidyl) Carbonate


Purity: >98.0%(T)
Synonyms:
  • N-Succinimidyl Carbonate
  • N,N'-Disuccinimidyl Carbonate
  • DSC
Product Documents:
5G
45,00 €
6   ≥80 
25G
146,00 €
16   13  

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Product Number D1662
Purity / Analysis Method >98.0%(T)
Molecular Formula / Molecular Weight C__9H__8N__2O__7 = 256.17 
Physical State (20 deg.C) Solid
Storage Temperature Refrigerated (0-10°C)
Store Under Inert Gas Store under inert gas
Condition to Avoid Moisture Sensitive,Heat Sensitive
CAS RN 74124-79-1
Reaxys Registry Number 1499137
PubChem Substance ID 87568139
MDL Number

MFCD00009767

Specifications
Appearance White to Light gray to Light yellow powder to crystal
Purity(Butylamine Method) min. 98.0 %
Properties (reference)
Melting Point 215 °C(dec.)
Solubility in water Insoluble
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H302 : Harmful if swallowed.
H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P501 : Dispose of contents/ container to an approved waste disposal plant.
P270 : Do not eat, drink or smoke when using this product.
P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P301 + P312 + P330 : IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell. Rinse mouth.
Related Laws:
EC Number 277-730-3
Transport Information:
HS Number 2925199590
Application
TCI Practical Example: Condensation Using Di(N-succinimidyl) Carbonate

TCI Practical Example: Condensation Using Di(N-succinimidyl) Carbonate

Used Chemicals

Procedure

To a solution of compound 3-(3,4-dimethoxyphenyl)propionic acid (0.10 g, 0.48 mmol), di(N-succinimidyl) carbonate (0.19 g, 0.62 mmol) in dichloromethane (5.0 mL) was added triethylamine (0.086 mL, 0.62 mmol) at ambient temperature and stirred at same temperature for 30 minutes. The mixture was added 4-methylbenzylamine (0.078 mL, 0.62 mmol) and stirred at same temperature for 1 hour. After completion of the reaction, the solvent was removed under reduced pressure and the residue was purified by column chromatography (ethyl acetate:hexane = 3:7 - 1:1 on silica gel) to give 1 (0.13 g,y. 86%) as a white solid.

Experimenter’s Comments

The reaction mixture was monitored by UPLC.

Analytical Data

compound 1

1H NMR (400 MHz, CDCl3); δ 7.10 (2H, d, J = 8.0 Hz), 7.05 (2H, d, J = 8.0 Hz), 6.78-6.70 (3H, m), 5.58 (1H, brs), 4.36 (2H, d, J = 5.6 Hz), 3.85 (3H, s), 3.83 (3H, s), 2.94 (2H, t, J = 7.6 Hz), 2.48 (2H, t, J = 7.6 Hz), 2.32 (3H, s).

Lead Reference

Other References


Application
A Condensing Reagent

Experimental procedure3): 1 (10 mg, 0.08 mmol) is dissolved in CH2Cl2 and, to this solution, Et3N (10 mg, 0.1 mmol) and N,N’-disuccinimidyl carbonate (26 mg, 0.1 mmol) are added. The resulting solution is stirred for 30 min after which ethanolamine (6 mg, 0.1 mmol) is added. The reaction is stirred at room temperature for an additional 1 hour. The organic solvent is evaporated and the residue is purified by preparative TLC (EtOAc) to afford 11 mg of compound 2 as a colorless oil, in 81% yield.

References


PubMed Literature


Product Documents (Note: Some products will not have analytical charts available.)
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