CAS 2446-83-5 Diso...

CAS 2446-83-5  Disopro′ ′ Pyl Azodicarboxylate
CAS 2446-83-5  Disopro′ ′ Pyl Azodicarboxylate
CAS 2446-83-5  Disopro′ ′ Pyl Azodicarboxylate
CAS 2446-83-5  Disopro′ ′ Pyl Azodicarboxylate
CAS 2446-83-5  Disopro′ ′ Pyl Azodicarboxylate

CAS 2446-83-5 Disopro′ ′ Pyl Azodicarboxylate

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Keywords

Diclofenac Sodium Powder CAS : 2446-83-5 2446-83-5

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  • Appearance:white Powder
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Hebei Mojin Biotechnology Co., Ltd,Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.

Adenosine triphosphate can be used in the disease caused by tissue injury and activity reduction of ecto enzyme , including heart failure, carditis, miocardial infarction, cerebral arteriosclersis, coronary sclerosis, progressive muscular atrophy , cerebral hemorrhage , chronic hepatitis, cirrhosis of liver and hearing handicap, etc.

 

 

 

 

 

 

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Product Detailed

Common Name Diiso''pro''pyl azodicarboxylate
CAS Number 2446-83-5 Molecular Weight 202.208
Density 1.2±0.1 g/cm3 Boiling Point 277.0±0.0 °C at 760 mmHg
Molecular Formula C8H14N2O4 Melting Point 3-5 °C

DIAD Alternative to DEAD (DIAD) is the di-isopropyl ester of azodicarboxylic acid. It is used as a reagent in the production of many organic compounds. It is often used in the Mitsunobu reaction where it serves as an oxidizer of triphenylphosphine to triphenylphosphine oxide. It has also been used to generate aza-Baylis-Hillman adducts with acrylates. It can also serve as a selective deprotectant of N-benzyl groups in the presence of other protecting groups.
It is sometimes preferred to diethyl azodicarboxylate (DEAD) because it is more hindered, and thus less likely to form hydrazide byproducts.

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