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61655-97-8

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61655-97-8 Usage

General Description

2,4-Dichloro-6-methylacetanilide is a chemical compound that belongs to the acetanilide group. It is commonly used as an herbicide to control broadleaf weeds in agricultural crops. The compound works by disrupting the growth of the weeds, leading to their eventual death. It is typically applied as a spray or as a component of a weed control mixture. However, it is important to handle this chemical with caution, as it can be toxic to humans and wildlife if not used properly. Overall, 2,4-Dichloro-6-methylacetanilide is an important tool in the agricultural industry for weed control, but its use should be carefully regulated to minimize environmental and health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 61655-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,5 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61655-97:
(7*6)+(6*1)+(5*6)+(4*5)+(3*5)+(2*9)+(1*7)=138
138 % 10 = 8
So 61655-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl2NO/c1-5-3-7(10)4-8(11)9(5)12-6(2)13/h3-4H,1-2H3,(H,12,13)

61655-97-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4-dichloro-6-methylphenyl)acetamide

1.2 Other means of identification

Product number -
Other names GNF-Pf-1679

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:61655-97-8 SDS

61655-97-8Synthetic route

4-chloro-2-methylacetanilide
5202-86-8

4-chloro-2-methylacetanilide

2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

Conditions
ConditionsYield
With chlorine; acetic acid
N-(2-methylphenyl)acetamide
120-66-1

N-(2-methylphenyl)acetamide

2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

Conditions
ConditionsYield
With chlorine; acetic acid
With ethanol; chlorine; acetic acid
With chlorine In chloroform; acetic acid Yield given;
ethanol
64-17-5

ethanol

N-(2-methylphenyl)acetamide
120-66-1

N-(2-methylphenyl)acetamide

acetic acid
64-19-7

acetic acid

2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

Conditions
ConditionsYield
Chlorieren;
p,N-dichloro-2'-methylacetanilide
230303-11-4

p,N-dichloro-2'-methylacetanilide

acetic acid
64-19-7

acetic acid

2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

4-chloro-2-methylacetanilide
5202-86-8

4-chloro-2-methylacetanilide

chlorine
7782-50-5

chlorine

acetic acid
64-19-7

acetic acid

2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

Conditions
ConditionsYield
Erwaermen des Reaktionsgemisches;
2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

2-methyl-4,6-dichloroaniline
30273-00-8

2-methyl-4,6-dichloroaniline

Conditions
ConditionsYield
With hydrogenchloride In ethanol for 18h; Heating;80%
With hydrogenchloride
With sulfuric acid
2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

acetic acid-(2,4,N-trichloro-6-methyl-anilide)

acetic acid-(2,4,N-trichloro-6-methyl-anilide)

Conditions
ConditionsYield
With acetic acid; calcium chloride
2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

3,5-dichloroantranilic acid
2789-92-6

3,5-dichloroantranilic acid

Conditions
ConditionsYield
durch Oxydation und Verseifung des Reaktionsproduktes;
2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

2,4-dichloro-6-methylbenzenediazonium tetrafluoroborate

2,4-dichloro-6-methylbenzenediazonium tetrafluoroborate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 80 percent / conc. aq. HCl / aq. ethanol / 18 h / Heating
2: 1.) conc. aq. HCl, NaNO2, 2.) NaBF4 / 1.) H2O, 5 deg C, 1 h, 2.) H2O
View Scheme
2,4-dichloro-6-methylacetanilide
61655-97-8

2,4-dichloro-6-methylacetanilide

3,5-dichlorotoluene
25186-47-4

3,5-dichlorotoluene

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: aq.-ethanolic sulfuric acid
2: NaNO2; aq.-ethanolic HCl / anschliessendes Erwaermen auf 60grad
View Scheme

61655-97-8Relevant articles and documents

Cardiotonic Agents. Synthesis and Cardiovascular Properties of Novel 2-Arylbenzimidazoles and Azabenzimidazoles

Guengoer, Timur,Fouquet, Andre,Teulon, Jean-Marie,Provost, Daniel,Cazes, Michele,et al.

, p. 4455 - 4463 (2007/10/02)

Novel 2-arylbenzimidazoles and azabenzimidazoles were synthesized, and their inotropic action was evaluated.Changes in left ventricular pressure, dP/dt max, were measured as an index of cardiac contractility.The structural features that impart optimal inotropic activity are presented.The most potent compounds were evaluated orally in conscious dogs with implanted Konigsberg pressure transducers.To investigate the mechanism of action, the most potent compounds were tested for their calcium-sensitizing properties and their potential for the inhibition of phosphodiesterase.Two compounds, 1 and 41, showed interesting in vitro and oral activity without side effects.They have a more potent calcium-sensitizing effect than MCI-154 and are under further investigation.

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