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Merck

323233

Oxalyl bromide solution

2.0 M in methylene chloride

Synonym(s):

Ethanedioyl dibromide solution, NSC 96957

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About This Item

Linear Formula:
BrCOCOBr
CAS Number:
Molecular Weight:
215.83
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
Form:
liquid
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form

liquid

Quality Segment

reaction suitability

reagent type: oxidant

concentration

2.0 M in methylene chloride

density

1.517 g/mL at 25 °C

functional group

acyl bromide

SMILES string

BrC(=O)C(Br)=O

InChI

1S/C2Br2O2/c3-1(5)2(4)6

InChI key

JAZLVNXWYDFQFE-UHFFFAOYSA-N

Application

Used in synthetic applications of carbon-substituted iminium salts

Reactant for:
  • Synthesis of mutasynthons added to cultures of A. pretiosum for mutasynthetic generation of ansamitocin derivatives
  • Oxalic acid formation from hydroxyl radical substitutions
  • Cyclization to produce CRF1 receptor antagonists
  • Preparation, optical and electrochemical studies of thiophene end capped olig(2,3-alkylthieno[3,4-b]pyrazine)
  • Asymmetrical synthesis of glycosyl chlorides and bromides


signalword

Danger

Hazard Classifications

Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Central nervous system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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