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OXALYL BROMIDE

  • Name OXALYL BROMIDE
  • CAS 15219-34-8
  • Purity 99%
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What is the OXALYL BROMIDE ?

OXALYL BROMIDE is clear yellow to yellow-green liquid, while it's Molecular Formula is C2Br2O2. 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 ratsfor validation of labelling for leptin-bearing cells of Sprague-Dawley ratsto study the effect of leptin on STAT3 (signal transducer and activator of transcription 3) phosphorylation in neural population of Sprague-Dawley ratsto study leptin response towards chemoreflex in nucleus of the solitary tractin rats, to check the effect of association between leptin and neuronal nitric oxide pathway on penicillin-induced epileptiform activity

What is the CAS number for OXALYL BROMIDE ?

The CAS number of OXALYL BROMIDE is 15219-34-8.

More information of OXALYL BROMIDE 15219-34-8 are:

Synonyms

OB;OXALYL BROMIDE;BrCOCOBr;Ethanedioyl bromide;ethanedioyldibromide;Ethanedioyl-dibromide-;OXALYL BROMIDE, 2.0M SOLUTION IN DICHLOR OMETHANE;Oxaly bromide

CAS?Number

15219-34-8

Molecular Formula

C2Br2O2

Molecular Weight

215.829

Density

2.627 g/cm3

Melting Point

-19 °C

Boiling Point

118.3 °C at 760 mmHg

Flash Point

109.8 °C

HS CODE

2917.19

PSA

34.14000

LogP

0.82940

What is OXALYL BROMIDE (15219-34-8) used for?

OXALYL BROMIDE is a clear yellow to yellow-green liquid that is commonly used in various synthetic applications and chemical reactions. It is known for its ability to facilitate the formation of carbon-substituted iminium salts and is involved in the synthesis of mutasynthons, which are added to cultures of A. pretiosum for mutasynthetic generation of ansamitocin derivatives. Additionally, OXALYL BROMIDE plays a role in the formation of oxalic acid from hydroxyl radical substitutions and is used in the cyclization process to produce CRF1 receptor antagonists. It is also utilized in the preparation, optical, and electrochemical studies of thiophene end-capped olig(2,3-alkylthieno[3,4-b]pyrazine) and in the asymmetrical synthesis of glycosyl chlorides and bromides.

InChI:InChI=1/C2Br2O2/c3-1(5)2(4)6

Articles related to OXALYL BROMIDE:

Article

Source

Element-organische Verbindungen; 9. Mitteilung. Synthese von Carbonsaeure-bromiden und Carbonsaeure-iodiden mit Hilfe von Halogentrimethylsilanen

Schmidt, Arthur H.,Russ, Manuel,Grosse, Detlef

, p. 216 - 218 (1981)

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