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3,7-Dichloro-8-chloro methyl quinoline, a chlorinated derivative of quinoline with the molecular formula C11H7Cl3N, is a chemical compound known for its potent fungicidal and pesticidal properties. Its unique structure, featuring three chlorine atoms and a chloromethyl group, endows it with broad-spectrum activity against various fungi and pests, making it a valuable asset in agricultural and industrial applications.

84086-96-4

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84086-96-4 Usage

Uses

Used in Agricultural Industry:
3,7-Dichloro-8-chloro methyl quinoline is used as a pesticide and fungicide for protecting crops from fungal infections. Its application helps in inhibiting the growth of fungi and preventing the development of fungal spores, thereby ensuring healthy crop growth and increased yield.
Used in Wood Treatment Industry:
In the wood treatment industry, 3,7-dichloro-8-chloro methyl quinoline is used as a preservative to prevent mold growth on wood surfaces. Its effective antifungal properties help in maintaining the structural integrity and longevity of wooden materials, making it suitable for applications such as construction, furniture making, and outdoor decking.
Used in Textile Industry:
3,7-Dichloro-8-chloro methyl quinoline is also utilized in the textile industry as a mold inhibitor. Its application on fabrics and textiles helps in preventing the growth of mold and mildew, thereby enhancing the durability and hygiene of the products. This is particularly important for items that are prone to moisture retention, such as carpets, upholstery, and outdoor clothing.
However, it is important to note that due to the potential toxicity and environmental impact of 3,7-dichloro-8-chloro methyl quinoline, its use is tightly regulated in many countries. Strict adherence to safety guidelines and regulations is necessary to minimize any adverse effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 84086-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,8 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84086-96:
(7*8)+(6*4)+(5*0)+(4*8)+(3*6)+(2*9)+(1*6)=154
154 % 10 = 4
So 84086-96-4 is a valid CAS Registry Number.

84086-96-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7,8-trichloro-2-methylquinoline

1.2 Other means of identification

Product number -
Other names 8-Chloromethyl-3,7-dichloroquinoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:84086-96-4 SDS

84086-96-4Synthetic route

7-Chloro-8-methylquinoline
78941-93-2

7-Chloro-8-methylquinoline

1,2-dichloro-benzene
95-50-1

1,2-dichloro-benzene

3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile); chlorine93%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

acetic acid
64-19-7

acetic acid

3,7-dichloro-quinoline-8-carboxylic acid
84087-01-4

3,7-dichloro-quinoline-8-carboxylic acid

Conditions
ConditionsYield
With hydrogen bromide; manganese (II) acetate tetrahydrate; cobalt(II) diacetate tetrahydrate at 150℃; under 7500.75 - 12001.2 Torr; for 4.2h; Concentration;96.2%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

sodium 4-chlorophenolate
1193-00-6

sodium 4-chlorophenolate

3,7-dichloro-8-p-chlorophenoxymethylquinoline
84087-06-9

3,7-dichloro-8-p-chlorophenoxymethylquinoline

Conditions
ConditionsYield
In N-methyl-acetamide; water95%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

3,7-dichloro-8-formylaminomethylquinoline
84087-08-1

3,7-dichloro-8-formylaminomethylquinoline

Conditions
ConditionsYield
In water; formamide94%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

3,7-dichloro-quinoline-8-carboxylic acid
84087-01-4

3,7-dichloro-quinoline-8-carboxylic acid

Conditions
ConditionsYield
With sodium tungstate (VI) dihydrate; copper(II) acetate monohydrate; cobalt(II) diacetate tetrahydrate; ozone In chlorobenzene at 110℃; for 8h;90.8%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

diethylamine
109-89-7

diethylamine

3,7-dichloro-8-diethylaminomethylquinoline

3,7-dichloro-8-diethylaminomethylquinoline

Conditions
ConditionsYield
In water89%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

3,7-dichloro-8-cyanoquinoline
88347-01-7

3,7-dichloro-8-cyanoquinoline

Conditions
ConditionsYield
With hydroxylamine hydrochloride; sodium formate In formic acid; water78.5%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

3,7-dichloro-8-cyanomethylquinoline
84087-00-3

3,7-dichloro-8-cyanomethylquinoline

Conditions
ConditionsYield
With potassium iodide In N-methyl-acetamide; water67%
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

3,7-dichloro-8-octylcarbonyloxymethylquinoline

3,7-dichloro-8-octylcarbonyloxymethylquinoline

Conditions
ConditionsYield
In water; dimethyl sulfoxide
3,7-dichloro-8-chloromethyl quinoline
84086-96-4

3,7-dichloro-8-chloromethyl quinoline

3,7-dichloro-8-[(2-nitrophenyl)-carbonyloxymethyl]-quinoline

3,7-dichloro-8-[(2-nitrophenyl)-carbonyloxymethyl]-quinoline

Conditions
ConditionsYield
In water; dimethyl sulfoxide

84086-96-4Relevant academic research and scientific papers

Dichloroquinoline derivatives for use as herbicides

-

, (2008/06/13)

Dichloroquinoline derivatives of the formula STR1 are prepared as described, and are used as herbicides.

3,7-Dichloroquinoline derivatives and their use for controlling undesirable plant growth

-

, (2008/06/13)

3,7-dichloroquinoline derivatives of the formula STR1 where R has the meanings given in the disclosure, a process for the preparation thereof, and their use for combating unwanted plant growth.

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