JPS5687536A - Monoterpenoid compound - Google Patents

Info

Publication number

JPS5687536A

JPS5687536A JP16455879A JP16455879A JPS5687536A JP S5687536 A JPS5687536 A JP S5687536A JP 16455879 A JP16455879 A JP 16455879A JP 16455879 A JP16455879 A JP 16455879A JP S5687536 A JPS5687536 A JP S5687536A

Authority

JP

Japan

Prior art keywords

formula

compound

tetramethylbicyclo

heptan

propionate

Prior art date

1979-12-18

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Pending

Links

• Espacenet
• Global Dossier
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• -1 Monoterpenoid compound Chemical class 0.000 title 1
• 229930003658 monoterpene Natural products 0.000 title 1
• GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 abstract 4
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
• MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 abstract 2
• 150000001875 compounds Chemical class 0.000 abstract 2
• GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 abstract 2
• OZBFUQLOVFXDNK-UHFFFAOYSA-N (4,6,6-trimethyl-2-bicyclo[3.1.1]hept-3-enyl) acetate Chemical compound CC(=O)OC1C=C(C)C2C(C)(C)C1C2 OZBFUQLOVFXDNK-UHFFFAOYSA-N 0.000 abstract 1
• SNMOQLYZFKYTMV-UHFFFAOYSA-N (4-ethyl-6,6-dimethyl-2-bicyclo[3.1.1]hept-3-enyl) propanoate Chemical compound CCC(=O)OC1C=C(CC)C2C(C)(C)C1C2 SNMOQLYZFKYTMV-UHFFFAOYSA-N 0.000 abstract 1
• DCSCXTJOXBUFGB-JGVFFNPUSA-N (R)-(+)-Verbenone Natural products CC1=CC(=O)[C@@H]2C(C)(C)[C@H]1C2 DCSCXTJOXBUFGB-JGVFFNPUSA-N 0.000 abstract 1
• DCSCXTJOXBUFGB-SFYZADRCSA-N (R)-(+)-verbenone Chemical compound CC1=CC(=O)[C@H]2C(C)(C)[C@@H]1C2 DCSCXTJOXBUFGB-SFYZADRCSA-N 0.000 abstract 1
• COBKZXSVCCODQR-UHFFFAOYSA-N 4,4,6,6-tetramethylbicyclo[3.1.1]heptan-2-one Chemical compound C1C2C(C)(C)C1C(=O)CC2(C)C COBKZXSVCCODQR-UHFFFAOYSA-N 0.000 abstract 1
• 241001674044 Blattodea Species 0.000 abstract 1
• XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
• WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 abstract 1
• 239000003513 alkali Substances 0.000 abstract 1
• SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 abstract 1
• 239000005667 attractant Substances 0.000 abstract 1
• 230000031902 chemoattractant activity Effects 0.000 abstract 1
• 229910000423 chromium oxide Inorganic materials 0.000 abstract 1
• JEHCHYAKAXDFKV-UHFFFAOYSA-J lead tetraacetate Chemical compound CC(=O)O[Pb](OC(C)=O)(OC(C)=O)OC(C)=O JEHCHYAKAXDFKV-UHFFFAOYSA-J 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 abstract 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
• DCSCXTJOXBUFGB-UHFFFAOYSA-N verbenone Natural products CC1=CC(=O)C2C(C)(C)C1C2 DCSCXTJOXBUFGB-UHFFFAOYSA-N 0.000 abstract 1

Cited By (1)