ChemicalBook--->CAS DataBase List--->15219-34-8

15219-34-8

15219-34-8 Structure

15219-34-8 Structure
IdentificationBack Directory
[Name]

OXALYL BROMIDE
[CAS]

15219-34-8
[Synonyms]

OB
CAD11
CDHOB
BrCOCOBr
NSC 96957
OXALYL BROMO
Oxaly bromide
OXALYL BROMIDE
Leptin from rat
Oxalyl dibromide
Oxalyl bromide,98%
Dibromoethanedione
Oxalyl broMide 97%
Ethanedioyl bromide
ethanedioyldibromide
Oxalic acid dibromide
Ethanedioyl-dibromide-
oxalyl bromide solution
Oxalyl broMide, 98% 25GR
Ethanedioyl dibromide solution
Anti-CDH11 antibody produced in goat
cadherin 11, type 2, OB-cadherin (osteoblast)
OXALYL BROMIDE, 2.0M SOLUTION IN DICHLOR OMETHANE
[EINECS(EC#)]

239-271-7
[Molecular Formula]

C2Br2O2
[MDL Number]

MFCD00000113
[MOL File]

15219-34-8.mol
[Molecular Weight]

215.83
Chemical PropertiesBack Directory
[Appearance]

clear yellow to yellow-green liquid
[Melting point ]

−19 °C(lit.)
[Boiling point ]

16-17 °C10 mm Hg(lit.)
[density ]

1.517 g/mL at 25 °C
[refractive index ]

n20/D 1.522(lit.)
[Fp ]

-19°C
[storage temp. ]

Refrigerator (+4°C)
[form ]

Liquid
[color ]

Clear
[BRN ]

1744437
[CAS DataBase Reference]

15219-34-8
[EPA Substance Registry System]

Ethanedioyl dibromide (15219-34-8)
Hazard InformationBack Directory
[Chemical Properties]

clear yellow to yellow-green liquid
[Uses]

Leptin 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
[Uses]

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
[Biochem/physiol Actions]

Leptin 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.
Safety DataBack Directory
[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
[F ]

8-9
[HazardClass ]

8
[PackingGroup ]

II
[HS Code ]

29171990
Spectrum DetailBack Directory
[Spectrum Detail]

OXALYL BROMIDE(15219-34-8)Raman
OXALYL BROMIDE(15219-34-8)FT-IR
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