589-21-9 | 4-Bromophenylhydrazine

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$10.00	$7.00
1g	98%	in stock	$13.00	$9.00
5g	98%	in stock	$29.00	$20.00
10g	98%	in stock	$56.00	$39.00
25g	98%	in stock	$116.00	$81.00

Description

• Catalog Number: AG66497
• Chemical Name: 4-Bromophenylhydrazine
• CAS Number: 589-21-9
• Molecular Formula: C6H7BrN2
• Molecular Weight: 187.03718
• MDL Number: MFCD01935685
• SMILES: NNc1ccc(cc1)Br
• NSC Number: 190724

Computed Properties

• Complexity: 79.1
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2.3

Upstream Synthesis Route

The (4-bromophenyl)-hydrazine is a versatile compound that finds wide application in chemical synthesis. It serves as a key building block in the preparation of various organic molecules due to its unique reactivity and functional groups. In synthetic organic chemistry, (4-bromophenyl)-hydrazine is commonly used in the formation of C-N bonds through coupling reactions with various electrophiles. Its ability to participate in nucleophilic substitution reactions also makes it valuable in the synthesis of heterocyclic compounds and pharmaceutical intermediates. Additionally, the presence of the bromine substituent provides a handle for further functionalization, enabling the introduction of additional chemical diversity.

Literature

• Competing intermolecular interactions in some 'bridge-flipped' isomeric phenylhydrazones.

  Acta crystallographica. Section C, Crystal structure communications 20120701

• (Z)-7-[2-(4-Bromo-phen-yl)hydrazin-1-yl-idene]-6-methyl-3-(pyridin-4-yl)-7H-1,2,4-triazolo[3,4-b][1,3,4]thia-diazine.

  Acta crystallographica. Section E, Structure reports online 20120501

• Microwave-assisted and continuous flow multistep synthesis of 4-(pyrazol-1-yl)carboxanilides.

  The Journal of organic chemistry 20110819

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• Spectrophotometric determination of V(V) in environmental, biological, pharmaceutical and alloy samples by novel oxidative coupling reactions.

  Journal of hazardous materials 20070209

• A new synthetic route to authentic N-substituted aminomaleimides.

  The Journal of organic chemistry 20050527

• [Induction of cell differentiation and development of new anticancer drugs].

  Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20020801

• Antitumor efficacy in vitro and in vivo of falconensones, a new type of polyene.

  Clinical cancer research : an official journal of the American Association for Cancer Research 20011101