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Assay
98%
mp
65-67 °C (lit.)
SMILES string
CCOC(=O)[C@@H](Br)CC[C@@H](Br)C(=O)OCC
InChI
1S/C10H16Br2O4/c1-3-15-9(13)7(11)5-6-8(12)10(14)16-4-2/h7-8H,3-6H2,1-2H3/t7-,8+
InChI key
UBCNJHBDCUBIPB-OCAPTIKFSA-N
General description
Diethyl meso-2,5-dibromoadipate reacts with N-methylallylamine in the presence of potassium carbonate to yield two diastereomers of diethyl 2-allyl-N-methylpyrrolidine-2,5-dicarboxylate.
Application
Diethyl meso-2,5-dibromoadipate may be employed as difunctional initiator during n-butyl acrylate (n-BuA) polymerization, leading to α,ω-bromo-poly(n-BuA) having narrow molecular weight distribution. It was also used:
- as bifunctional atom transfer radical polymerization (ATRP) initiator
- as initiator during the solution polymerization of octadecyl ester ether dimer by ATRP
- in the synthesis of diethyl 2,5-diazidoadipate
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Tandem cyclisation and [2, 3]-Stevens rearrangement to 2-substituted pyrrolidines.
Tetrahedron Letters, 43(5), 899-902 (2002)
ATOM TRANSFER RADICAL POLYMERIZATION OF OCTADECYL a-(HYDROXYMETHYL) ACRYLATE ESTER ETHER DIMER AND THEIR CORRESPONDING BLOCK COPOLYMERS.
Polymer Preprints (American Chemical Society, Division of Polymer Chemistry), 49(1), 416-416 (2008)
GRAFTING CARBOXYLIC ACIDS AND TERTIARY AMINES ONTO AZIDE-CONTAINING ALIPHATIC POLYESTERS.
Polymer Preprints (American Chemical Society, Division of Polymer Chemistry), 49(1), 181-181 (2008)
Effect of Block Order of ABA-and BAB-Type NIPAAm/HEMA Triblock Copolymers on Thermoresponsive Behavior of Solutions.
Macromolecular Chemistry and Physics, 208(16), 1773-1781 (2007)
Controlled radical polymerization of (meth) acrylates by ATRP with NiBr2 (PPh3) 2 as catalyst.
Macromolecules, 32(1), 27-35 (1999)
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