(2,5-Dibromophenyl)hydrazine
≥97%
- Product Code: 80227
CAS:
62672-26-8
Molecular Weight: | 265.95 g./mol | Molecular Formula: | C₆H₆Br₂N₂ |
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EC Number: | MDL Number: | MFCD02663135 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various heterocyclic compounds, which are essential in pharmaceutical and agrochemical industries. It is particularly valuable in the synthesis of indole derivatives, which have significant biological activities, including anti-inflammatory and anticancer properties. Additionally, it plays a role in the development of dyes and pigments, contributing to the coloration of materials in the textile and printing sectors. Its reactivity with carbonyl compounds also makes it useful in the preparation of hydrazones, which are employed in analytical chemistry for the detection and quantification of aldehydes and ketones.
Product Specification:
Test | Specification |
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APPEARANCE | White to Yellow solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $66.45 |
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1.000 | 10-20 days | $161.96 |
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(2,5-Dibromophenyl)hydrazine
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various heterocyclic compounds, which are essential in pharmaceutical and agrochemical industries. It is particularly valuable in the synthesis of indole derivatives, which have significant biological activities, including anti-inflammatory and anticancer properties. Additionally, it plays a role in the development of dyes and pigments, contributing to the coloration of materials in the textile and printing sectors. Its reactivity with carbonyl compounds also makes it useful in the preparation of hydrazones, which are employed in analytical chemistry for the detection and quantification of aldehydes and ketones.
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