71756-96-2

Basic information

• Product Name: 2,6-dibromo-4-fluorophenylnitramine
• CAS NO: 71756-96-2
• Molecular Weight: 313.908
• Mol File: 71756-96-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,6-dibromo-4-fluorophenylnitramine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dibromo-4-fluorophenylnitramine(71756-96-2)
• EPA Substance Registry System: 2,6-dibromo-4-fluorophenylnitramine(71756-96-2)

Safety Data

• Hazardous Substances Data: 71756-96-2(Hazardous Substances Data)

Upstream product

• 591-09-3 nitro acetate 
• 344-18-3 2,6-dibromo-4-fluoroaniline 
• 371-40-4 4-fluoroaniline 
• 351-83-7 4'-fluoroacetanilide 
• 393-42-0 2-amino-5-fluorobenzenesulfonic acid 

Downstream Products

• 1342817-87-1 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(3-bromophenyl)urea 
• 1342817-88-2 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(4-fluorophenyl)urea 
• 1342817-89-3 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(4-ethoxyphenyl)urea 
• 1342817-90-6 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(3,4-dimethoxyphenyl)urea 
• 1342817-91-7 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(2-methyl-3-chlorophenyl)urea 
• 1342817-92-8 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(2,4-dimethylphenyl)urea 
• 1342817-93-9 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(2,6-dimethylphenyl)urea 
• 1342817-94-0 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(3-methoxyphenyl)urea 
• 1342817-95-1 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(3,4-dimethylphenyl)urea 
• 1342817-96-2 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(4-methoxyphenyl)urea 
• 1342817-78-0 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(4-chlorophenyl)urea 
• 1342817-97-3 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(2,3-dimethylphenyl)urea 
• 1342817-98-4 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(2,5-dimethylphenyl)urea 
• 1342817-99-5 N-nitro-N-(2,6-dibromo-4-fluorophenyl)-N'-(1-napthyl)urea 

Relevant articles and documents

Cycloalkyl substituted N-nitrourea derivatives: A convenient synthesis and biological evaluation

A series of N-nitrourea derivatives bearing various cycloalkyl were conveniently obtained via three steps including nitration, carbamic chlorination, and aminolysis reactions. The structures of all newly synthesized compounds were elucidated and confirmed

Method for the control of stem growth and stem stiffness of graminaceous crops

The invention is a novel method for the control of the relative stem growth of graminaceous crops, comprising applying to the foliage, stems, roots or seeds of said plants, or to the soil in which said plants are grown, a plant growth regulating amount of