TH3028B - Pirazine compounds, their preparations and uses, mixtures containing them and methods for stopping unwanted plant growth. - Google Patents
Pirazine compounds, their preparations and uses, mixtures containing them and methods for stopping unwanted plant growth.Info
- Publication number
- TH3028B TH3028B TH8401000194A TH8401000194A TH3028B TH 3028 B TH3028 B TH 3028B TH 8401000194 A TH8401000194 A TH 8401000194A TH 8401000194 A TH8401000194 A TH 8401000194A TH 3028 B TH3028 B TH 3028B
- Authority
- TH
- Thailand
- Prior art keywords
- atoms
- compounds
- group
- selectable
- carbon atoms
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims 10
- 238000000034 method Methods 0.000 title claims 4
- 239000000203 mixture Substances 0.000 title claims 2
- 230000008635 plant growth Effects 0.000 title claims 2
- 238000002360 preparation method Methods 0.000 title claims 2
- 239000000126 substance Substances 0.000 claims abstract 7
- 125000004429 atom Chemical group 0.000 claims abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract 4
- 125000005842 heteroatom Chemical group 0.000 claims abstract 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 4
- 239000001301 oxygen Substances 0.000 claims abstract 4
- 239000011593 sulfur Chemical group 0.000 claims abstract 4
- 229910052717 sulfur Chemical group 0.000 claims abstract 4
- 229910052799 carbon Inorganic materials 0.000 claims abstract 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 3
- 239000004009 herbicide Substances 0.000 claims abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 2
- 229910052801 chlorine Inorganic materials 0.000 claims abstract 2
- 239000000460 chlorine Substances 0.000 claims abstract 2
- 229910052731 fluorine Inorganic materials 0.000 claims abstract 2
- 239000011737 fluorine Substances 0.000 claims abstract 2
- 230000002363 herbicidal effect Effects 0.000 claims abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 2
- 125000001624 naphthyl group Chemical group 0.000 claims abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- NYGHGTMKALXFIA-UHFFFAOYSA-N azapetine Chemical compound C1N(CC=C)CC2=CC=CC=C2C2=CC=CC=C21 NYGHGTMKALXFIA-UHFFFAOYSA-N 0.000 claims 1
- 229960004779 azapetine Drugs 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 238000003780 insertion Methods 0.000 claims 1
- 230000037431 insertion Effects 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 claims 1
- 229960003495 thiamine Drugs 0.000 claims 1
- 235000019157 thiamine Nutrition 0.000 claims 1
- 239000011721 thiamine Substances 0.000 claims 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 abstract 1
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Natural products C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- -1 pyrazine compound Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Abstract
สารประกอบพิราซีนที่มีสูตรทั่วไป (I) (สูตรเคมี) ซึ่ง X แทนออกซิเจน หรือกำมะถัน, R แทนไฮโดรเจน อะตอม หรือแอมโมเนียม แอลคิลที่มีคาร์บอนได้สูงถึง 6 อะตอม, หมู่เฟนิล หรือ เบนซิล, และ Y แทนหมู่แอโรมาทิค ที่เลือกได้จากเฟนิล, แนฟธิล และแอนธริล, หรือหมู่เฮเทอโรแอโร แอโรมาทิคที่มีอะตอมในริง 5 ถึง 6 อะตอม ซึ่งมีเฮเทอโรอะตอมได้สูงถึง 3 อะตอม ที่เลือกได้จากไนโตรเจน, ออกซิเจน และกำมะถัน,หมู่แอโรมาทิค หรือเฮเทอโรแอโรมาทิค ดังกล่าวไม่เป็นชนิดที่ถูกแทนที่หรือเป็นชนิดที่ถูกแทนที่ ได้โดยหมู่แทนที่ 1 หรือ 2 หมู่ ที่อิสระต่อกันซึ่งเลือกได้จาก ไซแอโน, เฮโล,อะมิโน, ไบโทร, แอลคอกซิที่มีคาร์บอนได้สูงถึง 4 อะตอม,เฮโลแอลคอกซิ และเฮโลแอลคิลที่มีคาร์บอนได้สูงถึง4 อะตอม แลมีโบรมีน, คลอรีน หรือฟลูออรีนได้สูงถึง 4 อะตอม และแอลคิลที่มีคาร์บอนได้สูงถึง 4 อะตอม หรือที่ตำแหน่งอยู่ติดๆ กันโดยหมู่ชนิดไบวาเลนท์ (สูตรเคมี) ซึ่ง n เป็น 1 หรือ 2 มีคุณสมบัติฆ่าวัชพืชซึ่งใช้เป็นประโยชน์ได้ A pyrazine compound with the general formula (I) (chemical formula), where X represents oxygen or sulfur, R represents hydrogen atoms, or ammonium. Alkyl with up to 6 carbon atoms, phenyl group or benzyl group, and Y represents the aromatic group. Selectable from phenyl, naphthyl and anthrill, or heteroaroe groups. Aeromatics with 5 to 6 atoms in the ring, up to 3 hetero atoms, selectable from nitrogen, oxygen and sulfur, aeromatic groups. or hetero-aromatic It is not a superseded type or a superseded type. can be obtained by 1 or 2 independent substituent groups which can be selected from cyano, halo, amino, bitro, up to 4 carbon alkoxy, haloalcox and haloalkyl with up to 4 carbon atoms, lamebromine, chlorine or fluorine up to 4 atoms and alkyl with up to 4 carbon atoms or adjacent locations. It is classified by the bivalent group (chemical formula), where n is 1 or 2, which has useful herbicide properties.
Claims (1)
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH1950A TH1950A (en) | 1984-11-01 |
| TH3028B true TH3028B (en) | 1992-08-07 |
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