IP Library › Granted Patent US 7,572,753
Granted Patent B2
US 7,572,753 · App. 11/228,653 · Granted Aug 11, 2009

Tetrazole fungicides

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Quick Facts
Patent No.
US 7,572,753
App. No.
11/228,653
Granted
Aug 11, 2009
Kind
B2
Abstract

The use of certain tetrazole compounds as fungicides is disclosed wherein said compounds are of the structural formula: wherein: R is selected from the group consisting of phenyl groups of the structural formula: and thienyl groups of the structural formula: and X and Y are each selected from the group consisting of hydrogen, haloalkyl, halogen, and nitro. Novel compounds wherein X is selected from the group consisting of haloalkyl, halogen, and nitro and Y is selected from the group consisting of hydrogen, haloalkyl, halogen, and nitro are also disclosed.

Claims (36)

1. A tetrazole compound of the structural formula:

wherein:

R is selected from the group consisting of phenyl groups of the structural formula:

and thienyl groups of the structural formula:

X is selected from the group consisting of haloalkyl, halogen, and nitro, and

Y is selected from the group consisting of hydrogen, haloalkyl, halogen, and nitro.

2. The compound of claim 1 wherein Y is selected from the group consisting of haloalkyl, halogen, and nitro.

3. The compound of claim 1 wherein said compound is of the structure:

wherein Y′ is chlorine or bromine.

4. A composition comprising

(A) a fungicidally effective amount of a tetrazole compound of the structural formula:

wherein:

R is selected from the group consisting of phenyl groups of the structural formula:

and thienyl groups of the structural formula:

X is selected from the group consisting of haloalkyl, halogen, and nitro, and Y is selected from the group consisting of hydrogen, haloalkyl, halogen, and nitro; and

(B) a suitable carrier.

5. The composition of claim 4 wherein R is a substituted phenyl group and X is selected from the group consisting of haloalkyl, halogen, and nitro.

6. The composition of claim 4 wherein R is a substituted thienyl group and Y is selected from the group consisting of haloalkyl, halogen, and nitro.

7. The composition of claim 4 wherein the tetrazole compound is of the structure:

wherein Y′ is chlorine or bromine.

8. A tetrazole of the structural formula:

wherein:

R is selected from the group consisting of phenyl groups of the structural formula:

and thienyl groups of the structural formula:

X is selected from the group consisting of haloalkyl, halogen, and nitro, and

Y is selected from the group consisting of haloalkyl, halogen, and nitro.

9. The compound of claim 8 , wherein the tetrazole compound is of the structure:

wherein Y′ is chlorine or bromine.

10. A composition comprising

(A) a fungicidally effective amount of a tetrazole compound of the structural formula:

wherein:

R is a thienyl group of the structural formula:

Y is selected from the group consisting of haloalkyl, halogen, and nitro; and

(B) a suitable camer.

11. The composition of claim 10 , wherein the tetrazole compound is of the structure:

wherein Y′ is chlorine or bromine.

Assignments (4)
RELEASE OF FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042447/0508 →
RELEASE OF SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042449/0001 →
FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT. Recorded Mar 21, 2011
From: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 026028/0622 →
INTELLECTUAL PROPERTY SECURITY RELEASE AGREEMENT Recorded Mar 21, 2011
From: CITIBANK, N.A.
To: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; ASCK, INC; BIOLAB COMPANY STORE, LLC; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIOLAB TEXTILES ADDITIVES, LLC; BIOLAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON MONOCHEM, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GT SEED TREATMENT, INC.; ISCI, INC; GREAT LAKES CHEMICAL GLOBAL, INC.; HOMECARE LABS, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; NAUGATUCK TREATMENT COMPANY; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); MONOCHEM, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC; WRL OF INDIANA, INC.; BIOLAB FRANCHISE COMPANY, LLC
Reel/Frame 026039/0142 →