84478-65-9

Basic information

• Product Name: Benzenamine, 4-chloro-2-fluoro-5-(2-propynyloxy)-
• CAS NO: 84478-65-9
• Molecular Formula: C9H7ClFNO
• Molecular Weight: 199.612
• Mol File: 84478-65-9.mol

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-chloro-2-fluoro-5-(2-propynyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-chloro-2-fluoro-5-(2-propynyloxy)-(84478-65-9)
• EPA Substance Registry System: Benzenamine, 4-chloro-2-fluoro-5-(2-propynyloxy)-(84478-65-9)

Safety Data

• Hazardous Substances Data: 84478-65-9(Hazardous Substances Data)

Upstream product

• 7439-89-6 iron 
• 143659-40-9 bis(2-chloro-4-fluoro-5-aminophenyl) carbonate 
• 106-96-7 propargyl bromide 
• 158174-63-1 3-amino-6-chloro-4-fluorophenol hydrochloride 

Downstream Products

• 84478-42-2 S-23142 
• 1041682-56-7 C₁₆H₁₄ClFN₄O₂ 
• 1041681-92-8 C₁₆H₁₁ClFN₅O₂ 
• 1041681-94-0 C₁₆H₁₁ClFN₅O₂ 
• 1041682-35-2 C₁₅H₁₁ClF₄N₄O₂ 
• 125318-61-8 4-chloro-2-fluoro-5-cyclopentyloxycarbonylmethylthiophenylisothiocyanate 
• 161679-29-4 4-chloro-2-fluoro-5-pentyloxycarbonylmethoxyphenylisothiocyanate 
• 85953-27-1 1-chloro-5-fluoro-4-isocyanato-2-(2-propynyloxy)benzene 
• 134814-95-2 N-(4'-chloro-2'-fluoro-5'-propargyloxyphenyl)-3-(trifluoromethyl)glutaramic acid 

Relevant articles and documents

Heterocyclic herbicides

Compounds of Formula I, and their N-oxides and agriculturally suitable salts, are disclosed which are useful for controlling undesired vegetation wherein, Q is and W,X,R1-R7are as defined in the disclosure. Also disclosed are composi

Process for the production of aniline derivatives

Industrial process for the efficient production of aniline derivatives which are important intermediates for the manufacture of oxazolidinedione derivatives and tetrahydrophthalimide derivatives which are useful as active ingredients of herbicides. The process starts from 2,4-dihalo-5-aminophenol or bis(2,4-dihalo-5-aminophenyl)carbonate and selectively cycloalkylates or alkynylates the hydroxy group without protecting the amino group, whereby aniline derivatives having the cycloalkyloxy group or alkynyloxy group can be produced in high yield.

Herbicidal imidazolones

Compounds such as Formula I having herbicidal utility are disclosed: STR1 wherein Q is STR2 R1 is H; alkyl, haloalkyl or halogen R2 is C1 -C2 alkyl optionally substituted with one or more halogens, OR8, CN, COR9, CO2 R31 or CONR32 R33 ; CN; CO2 R34 ; CONR35 R36 ; S(O)n R8 ; S(O)n NR19 R8 or COR37 ; or R1 and R2 can be taken together along with the carbon to which they are attached to form C=CHCO2 R31 ; C=(CH3)CO2 R31 ; C=(C2 H5)CO2 R31 ; C=CHCONR32 R33 ; C=C(CH3)CONR32 R33 or C=C(C2 H5)CONR32 R33.

Herbicidal glutaramic acids and derivatives

This invention relates to glutaramic acids and derivatives exhibiting herbicidal activity having the structure STR1 wherein A is a carboxylic acid or a derivative thereof, D is CH or N, and R, R1, R2, T, X, Y, and Z are as defined within, compositions containing these compounds and methods of controlling weeds with these compounds.

N-(2-Fluoro-4-halo-5-substituted phenyl) hydantoins

A composition comprising an N-(2-fluoro-4-halo-5-substituted phenyl) hydantoin of the formula: STR1 wherein X is a chlorine atom or a bromine atom and R1 and R2 are, same or different, each a C1 -C4 alkyl group, a cyclopropyl group, a C3 -C4 alkenyl group or a C3 -C4 alkynyl group and an inert carrier, which is useful as a herbicide.

4-(2-Fluoro-4-halo-5-substituted phenyl)urazols, and their production and use

A condensed phenylurazol of the formula: STR1 wherein X is a chlorine atom or a bromine atom, Y and Z are each an oxygen atom or a sulfur atom and R is a C1 -C3 alkyl group, an allyl group or a propargyl group and n is an integer of 4 or 5, which is useful as a herbicide.

2-(2-Fluoro-4-halo-5-substituted phenyl) hydantoins and use

A herbicidal composition which comprises as an active ingredient a compound of the formula: STR1 wherein X is a chlorine atom or a bromine atom, Y is --CH2 --, --S-- or --SO2 -- and R is a C1 -C4 alkyl group, an allyl group or a propargyl group, and an inert carrier.