Interesting facts
Interesting Facts About 2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)acetamide
This compound, with a structurally complex name, belongs to a class of molecules known for their diverse biological activity. Here are some engaging insights about it:
- Utility in Pharmaceuticals: Compounds of this nature are often investigated in drug development. The presence of a chloro group can enhance the compound's lipophilicity, potentially leading to improved biological efficacy.
- Structure-Activity Relationship (SAR): The intricate structure highlights the significance of functional groups. Chemists frequently explore how the various substituents affect the compound's interaction with biological targets. For instance, the ethyl and methyl groups can influence the compound's hydrophobic character.
- Reactivity: Compounds with halogen atoms, such as chlorine, can undergo nucleophilic substitution reactions, leading to further chemical transformations. This aspect makes them essential in synthetic chemistry.
- Environmental Impact: The study of compounds like this one not only focuses on their medicinal properties but also on their environmental degradation and persistence. Understanding their behavior in the environment is crucial for assessing ecological risks.
- Multidisciplinary Interest: The chemistry of this compound crosses various scientific disciplines, including organic chemistry, pharmacology, and environmental science. This interdisciplinary relevance showcases the broader impact of researching such chemical entities.
As scientists delve into the properties and applications of 2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)acetamide, they contribute to the ongoing discovery of compounds that may lead to revolutionary therapies and insights in chemical science.
Synonyms
metolachlor
51218-45-2
Pennant
Yibingjiacaoan
Codal
Dual
Dual Magnum
Dual Triple
Metelilachlor
Dual II
2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide
Ontrack 8E
Dual 720EC
Humextra
Dual 8E
Dual 960 EC
Metolachlor technical
Metetilachlor
Metolachlore
Jindual
Metoken
2-Chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide
Metolachlor [ISO]
N-(1-Methyl-2-methoxyethyl)-N-chloroacetyl-2-ethyl-6-methylaniline
CGA 24705
CGA-24705
Acetamide, 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)-
METOLACHOR
DTXSID4022448
X0I01K05X2
METOLACHLOR [MI]
METOLACHLOR [HSDB]
DTXCID402448
CHEBI:83645
Metolachlor, herbicide (C15-H22-N-O2-Cl)
2-Chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)-o-acetotoluidine
82535-90-8
2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)acetamide
Acetamide,2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)-
Acetamide, 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)-, stereoisomer
Caswell No. 188DD
2-CHLORO-6-ETHYL-N-(2-METHOXY-1-METHYLETHYL)ACET-O-TOLUIDIDE
Metolachlore [ISO-French]
.ALPHA.-CHLORO-2-ETHYL-6-METHYL-N-(1-METHYL-2-METHOXYETHYL)ACETANILIDE
CAS-51218-45-2
Metolachlor [ANSI:BSI:ISO]
HSDB 6706
EINECS 257-060-8
EPA Pesticide Chemical Code 108801
BRN 2743537
Metolaclor
Pimagram
UNII-X0I01K05X2
Bicep 6L
Bicep (Salt/Mix)
Turbo (Salt/Mix)
CGA-77102
MFCD00055293
Pace 6L
Dual 25G
Primagram (Salt/Mix)
Primextra (Salt/Mix)
(aS,5S)-Metolachlor
Spectrum_001833
Metolaclor (Salt/Mix)
SpecPlus_000434
2-Chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)acet-o-toluidide
Pace 6L (Salt/Mix)
Bicep 6L (Salt/Mix)
2-Ethyl-6-methyl-1-N-(2-methoxy-1-methylethyl)chloroacetanilide
Spectrum2_001885
Spectrum3_000827
Spectrum4_000667
Spectrum5_001966
2-Aethyl-6-methyl-N-(1-methyl-2-methoxyaethyl)-chloracetanilid [German]
Acetamide, 2-chloro-N-(6-ethyl-o-tolyl)-N-(2-methoxy-1-methylethyl)-
Dual 25G (Salt/Mix)
N-(2'-Methoxy-1'-methylethyl)-2'-ethyl-6'-methyl-2-chloroacetanilide
2-Etylo-6-metylo-N-(1'-metylo-2'-metoksyetylo)chloroacetanilid [Polish]
alpha-Chlor-6'-aethyl-N-(2-methoxy-1-methylaethyl)-acet-o-toluidin [German]
alpha-Chloro-2'-ethyl-6'-methyl-N-(1-methyl-2-methoxyethyl)-acetanilide
Metolachlor standard solution
SCHEMBL21385
BSPBio_002353
KBioGR_001073
KBioSS_002338
SPECTRUM330035
DivK1c_006530
SPBio_001790
CHEBI:6902
Metolachlor, analytical standard
CHEMBL1884974
KBio1_001474
KBio2_002335
KBio2_004903
KBio2_007471
KBio3_001853
2-Aethyl-6-methyl-N-(1-methyl-2-methoxyaethyl)-chloracetanilid
2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxyethyl)acetamide
2-Etylo-6-metylo-N-(1'-metylo-2'-metoksyetylo)chloroacetanilid
BCA21845
CGA24705
HY-B1871
MSK22402
UYB80397
Tox21_201376
Tox21_300982
alpha-Chlor-6'-aethyl-N-(2-methoxy-1-methylaethyl)-acet-o-toluidin
CCG-39423
o-Acetotoluidide, 2-chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)-
AKOS015888371
Acetamide, 2-chloro-N-(2-ethyl-6-methylphenyl)-N-((1S)-2-methoxy-1-methylethyl)-, (N(S))-
Metolachlor 1000 microg/mL in Acetone
USEPA/OPP Pesticide Code: 108801
Metolachlor 10 microg/mL in Cyclohexane
NCGC00095767-01
NCGC00095767-02
NCGC00095767-03
NCGC00095767-04
NCGC00095767-05
NCGC00095767-06
NCGC00254884-01
NCGC00258927-01
BS-42451
Metolachlor 10 microg/mL in Acetonitrile
Metolachlor 100 microg/mL in Cyclohexane
Metolachlor 100 microg/mL in Acetonitrile
DB-051924
CS-0013937
M3381
NS00000248
E84049
Metolachlor, PESTANAL(R), analytical standard
EN300-18537345
Q409598
2Chloro6'ethylN(2methoxy1methylethyl)acetotoluidide
2Chloro6'ethylN(2methoxy1methylethyl)oacetotoluidine
2Aethyl6methylN(1methyl2methoxyaethyl)chloracetanilid
2Ethyl6methyl1N(2methoxy1methylethyl)chloroacetanilide
2Etylo6metyloN(1'metylo2'metoksyetylo)chloroacetanilid
alphaChlor6'aethylN(2methoxy1methylaethyl)acetotoluidin
BRD-A43135847-001-02-3
oAcetotoluidide, 2chloro6'ethylN(2methoxy1methylethyl)
Acetamide, 2chloroN(6ethylotolyl)N(2methoxy1methylethyl)
N(1Methyl2methoxyethyl)Nchloroacetyl2ethyl6methylaniline
Z3234876186
alphaChloro2'ethyl6'methylN(1methyl2methoxyethyl)acetanilide
N(2'Methoxy1'methylethyl)2'ethyl6'methyl2chloroacetanilide
2ChloroN(2ethyl6methylphenyl)N(2methoxy1methylethyl)acetamide
2-chloro-2'-ethyl-6'-methyl-N-(1-methyl-2-methoxyethyl)acetanilide
2-chloro-6'-ethyl-n-(2-methoxy-1-methylethyl)aceto-o-toluidide
2-chloro-2'-ethyl-6'-methyl-N-(1-methyl-2-methoxyethyl)-acetanilide
2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(1-methoxypropan-2-yl) acetamide
alpha-Chloro-2'-ethyl-6'-methyl-N-(1-methyl-2-methoxyethyl)acetanilide
rac-2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide
2-Chloro-N-(2-ethyl-6-methylphenyl)-N-[1-(methoxymethyl-d2)ethyl-1,2,2,2-d4]acetamide
ALPHA-CHLORO-2-ETHYL-6-METHYL-N-(1-METHYL-2-METHOXYETHYL)ACETANILIDE
257-060-8
Solubility of 2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)acetamide
The solubility of the compound 2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)acetamide (C15H22ClNO2) is influenced by several factors, given its unique structure. This compound features a chloro group, an acetamide moiety, and bulky alkyl substituents, which collectively affect its interaction with solvents.
Factors Influencing Solubility:
In essence, while C15H22ClNO2 may exhibit moderate solubility in polar solvents due to its slightly polar functional groups, it is likely to be more soluble in organic solvents due to its hydrophobic characteristics. Therefore, the most effective solvents for achieving dissolution will typically include:
Understanding the solubility profile is crucial for applications in fields such as pharmaceuticals, where the behavior of the compound in different solvents can influence formulation, absorption, and overall efficacy.