Detail of > 38727-55-8
- CAS Number:
- 38727-55-8
- Name:
Glycine,N-(2-chloroacetyl)-N-(2,6-diethylphenyl)-, ethyl ester
- Formula:
- C16H22 Cl N O3
- Molecular Structure:

- Synonyms:
- Glycine,N-(chloroacetyl)-N-(2,6-diethylphenyl)-, ethyl ester (9CI);Antor;Bay NNT6867;Diethacine-ethyl;Diethatyl-ethyl;EthylN-(2,6-diethylphenyl)-N-(chloroacetyl)aminoacetate;EthylN-chloroacetyl-2,6-diethylanilinoacetate;H 22234;Hercules 22234;N-Chloroacetyl-N-(2,6-diethylphenyl)glycine ethyl ester;Nevirex G;
- Molecular Weight:
- 311.8038
- EINECS:
- 254-105-3
- Density:
- 1.15 g/cm3
- Boiling Point:
- 447.9 °C at 760 mmHg
- Flash Point:
- 224.7 °C
- Deleted CAS:
- 62180-86-3
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Reference
- Metabolism of two new acylanilide herbicides, Antor herbicide (H-22234) and Dual (metolachlor) by the soil fungus Chaetomium globosum
- Metabolism of two new acylanilide herbicides, Antor herbicide (H-22234) and Dual (metolachlor) by the soil fungus Chaetomium globosum. McGahen, Linda L.; Tiedje, James M. (Dep. Crop Soil Sci., Michigan State Univ., East Lansing, Mich., USA). J. Agric.There are some reagents like 65513-68-0 is used in this study. Food Chem., 26(2), 414-19 (English) 1978. CODEN: JAFCAU. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) The metab. of Antor herbicide (I) [38727-55-8] and Dual (II) [51218-45-2] by resting C. globosum was studied. At least 10 products were obsd. with I as the substrate and at least 8 with II. The products of I, identified by gas chromatog.-mass spectrometry using electron and chem. ionization were: 2-chloro-N-(2,6-diethylphenyl)acetamide [6967-29-9], 2-hydroxy-N-(2-ethyl-6-vinylphenyl)-N-methyl(ethyl carboxylate)acetamide [65513-57-7], Et 7-ethyl-2,3-dihydroindoxyacetate [65513-58-8], 2-chloro-N-(2-ethyl-6-vinylphenyl)-N-methyl(ethyl carboxylate)acetamide [65513-59-9], and Et 2,6-diethylphenyliminoacetate [65513-60-2]. Compds. produced from II were: 2-chloro-N-(2-ethyl-6-methylphenyl)acetamide [32428-71-0] and 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-hydroxy-1-methylethyl)acetami de [65513-61-3]. Generally, C. globosum removes 1 or both of the R groups from the N, dehydrogenates the Et substituent, and in some cases forms an indoline ring. It may also remove the chloro, methoxy, or ethoxy substituent from the R groups with subsequent hydroxylation at that position. .
- Control of Apera spica venti and Alopecurus myosuroides in winter cereals
- Control of Apera spica venti and Alopecurus myosuroides in winter cereals. Aamisepp, Ants (Dep. Plant Husb., Agric. Coll. Swed., Uppsala, Swed.). Swed. Weed Conf., [Proc.], 18(Weeds Weed Control), F9-F13 (English) 1977. CODEN: SWDCAZ. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemicals) Good control of Apera spica venti in winter cereals was obtained with Tribunil (I) [18691-97-9] (30 kg/ha), Sinadal 3622 [8068-87-9] (2.5 kg/ha), Dosanex (II) [19937-59-8] (3.0 kg/ha), Arelon (III) [34123-59-6] 2.0-3.0 kg/ha), Hercules 22234 (IV) [38727-55-8] (4.0 L/ha), or Stomp [40487-42-1] (6.0 L/ha) applied after sowing and moderate to good yields were obtained with spring application of Hoe 17014 [20782-58-5] (2.5-3.5 kg/ha), or I (3.0 kg/ha) or III (2.5-3.0 kg/ha). Moderate to good control of Alopecurus myosuroides in winter cereals were obtained with fall applications of I (4.0 kg/ha), II (3.0 kg/ha), III (2.0-3.0 kg/ha), IV (5.0 L/ha) or Trinulan [8070-92-6] (5.0 L/ha). Spring application of I (3 kg/ha), III (2.0-3.0 kg/ha), and Hoe 22870 (V) [51337-71-4] (1.0-2.0 L/ha) gave moderate to very good control.
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