OXALYL BROMIDE

OXALYL BROMIDE Basic information
Product Name:OXALYL BROMIDE
Synonyms:oxalyl bromide solution;OXALYL BROMO;BrCOCOBr;Ethanedioyl bromide;ethanedioyldibromide;Ethanedioyl-dibromide-;OXALYL BROMIDE, 2.0M SOLUTION IN DICHLOR OMETHANE;Dibromoethanedione
CAS:15219-34-8
MF:C2Br2O2
MW:215.83
EINECS:239-271-7
Product Categories:Others;Oxidation;Synthetic Reagents
Mol File:15219-34-8.mol
OXALYL BROMIDE Structure
OXALYL BROMIDE Chemical Properties
Melting point -19 °C (lit.)
Boiling point 16-17 °C/10 mmHg (lit.)
density 1.517 g/mL at 25 °C
refractive index n20/D 1.522(lit.)
Fp -19°C
storage temp. 2-8°C
solubility Benzene (Slightly), Chloroform
form Liquid
color Clear
BRN 1744437
Stability:Moisture Sensitive
CAS DataBase Reference15219-34-8
EPA Substance Registry SystemEthanedioyl dibromide (15219-34-8)
Safety Information
Hazard Codes C,T
Risk Statements 23/24/25-34-40-29-20-14-37
Safety Statements 26-36/37/39-45-28-27
RIDADR UN 3265 8/PG 2
WGK Germany 3
8-9
HazardClass 8
PackingGroup II
HS Code 29171990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
OXALYL BROMIDE Usage And Synthesis
Chemical Propertiesclear yellow to yellow-green liquid
UsesUsed 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
UsesLeptin from rat has been used:
  • to check the effect of intranasal nerve growth factor (NGF) on NGF activity in the spinal cord of Sprague-Dawley rats
  • for validation of labelling for leptin-bearing cells of Sprague-Dawley rats
  • to study the effect of leptin on STAT3 (signal transducer and activator of transcription 3) phosphorylation in neural population of Sprague-Dawley rats
  • to study leptin response towards chemoreflex in nucleus of the solitary tract
  • in rats, to check the effect of association between leptin and neuronal nitric oxide pathway on penicillin-induced epileptiform activity
Biochem/physiol ActionsLeptin is a hormone produced primarily in adipocytes, although leptin mRNA has also been identified in placenta and fetal tissues, gastric tissue and liver. Its primary site of action appears to be on neurons in the hypothalamus that are involved in regulating energy balance, appetite, and body weight. Leptin increases the production of nitric oxide in endothelial cells and stimulates angiogenesis in vitro and in vivo.Human and mouse leptin share ~84% sequence identity.
Aluminum Bromide Trisodium phosphate Ferric nitrate Mercury Lactic acid 2-Bromoisobutyryl Bromide OXALYL BROMIDE Glyoxal Bromoacetaldehyde Acetyl bromide Formaldehyde 1,2-Dibromoethane Bromoacetyl bromide Bromoethane

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