ClassID:

90812

C07C13/20 - CPC Classification

Classification description:

Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings; Monocyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with a six-membered ring with a cyclohexene ring

Sub-classes:
Recent Application in this class:
#1
20250304517
2025-10-02

STERIOISOMER-SPECIFIC CANNABIS FORMULATIONS AND ANALYSIS

#2
20240076252
2024-03-07

Preparation process of 5-ethylidene-2-norbornene

#3
20230391904
2023-12-07

Biobased materials derived from cyclic monoterpenes

#4
20220204430
2022-06-30

STEREOISOMER-SPECIFIC CANNABIS FORMULATIONS AND ANALYSIS

#5
20210339164
2021-11-04

LIQUID PRODUCTION METHOD AND LIQUID PRODUCTION DEVICE

#6
20190292200
2019-09-26

Method for preparing 2-(cyclohexenylidene) malonic acid derivatives and uses thereof

#7
20190203232
2019-07-04

Production of monoterpene blends by unicellular photosynthetic microorganisms

#8
20190201877
2019-07-04

MIXED METAL IRON OXIDES AND USES THEREOF

#9
20190194158
2019-06-27

Arthropod repellent chemicals

#10
20180094115
2018-04-05

Curable compositions containing 1,1-di-activated vinyl compounds that cure by pericyclic reaction mechanisms

#11
20180065114
2018-03-08

Mixed metal iron oxides and uses thereof

#12
20170369468
2017-12-28

ANTHROPOD REPELLENT CHEMICALS

#13
20170327439
2017-11-16

Dihydronaphthalene derivative

#14
20170313654
2017-11-02

Process of production of 7,8-dihydro-C15-aldehyde

#15
20170297971
2017-10-19

Method for marking oil products and marker composition for oil products

#16
20160272612
2016-09-22

ANTHROPOD REPELLENT CHEMICALS

#17
20150251996
2015-09-10

PROCESS FOR THE PRODUCTION OF 1,3,3-TRIMETHYL-2-(3-METHYLPENT-2-EN-4-YNYL)CYCLOHEX-1-ENE

#18
20150133627
2015-05-14

Methods of preparing para-xylene from biomass

#19
20140081058
2014-03-20

Methods for high yield production of terpenes

#20
20140017744
2014-01-16

Methods of preparing -xylene from biomass

#21
20130131418
2013-05-23

Mesoporous carbon supported copper based catalyst, production and use thereof

#22
20120264988
2012-10-18

Cineole

#23
20120238792
2012-09-20

Deoxygenation process

#24
20120083637
2012-04-05

Regeneration of metal-containing catalysts

#25
20110282068
2011-11-17

Alkylidene complexes of ruthenium containing N-heterocyclic carbene ligands; use as highly active, selective catalysts for olefin metathesis

#26
20110259242
2011-10-27

Additives to prevent degradation of cyclic alkene derivatives

#27
20110257449
2011-10-20

Method for preparing ruthenium catalyst for producing cycloolefin and method and apparatus for producing cycloolefin

#28
20110178199
2011-07-21

Method for producing organic compound and organic compound obtained by the method

#29
20110091651
2011-04-21

Additives to prevent degradation of cyclic alkene derivatives

#30
20100197988
2010-08-05

Method for separating and producing cyclohexene

#31
20100168454
2010-07-01

Catalytic hydrogenation

#32
20090291210
2009-11-26

Additives to prevent degradation of cyclic alkene derivatives

#33
20080207911
2008-08-28

ALKYLIDENE COMPLEXES OF RUTHENIUM CONTAINING N-HETEROCYCLIC CARBENE LIGANDS; USE AS HIGHLY ACTIVE, SELECTIVE CATALYSTS FOR OLEFIN METATHESIS

#34
20080064908
2008-03-13

Catalyst for cycloolefin production and process for production

#35
20080009598
2008-01-10

Alkylidene complexes of ruthenium containing N-heterocyclic carbene ligands; use as highly active, selective catalysts for olefin metathesis

#36
20060287450
2006-12-21

Immobilizable ruthenium catalysts having n-heterocyclic carbene ligands

#37
20060252951
2006-11-09

Process for continuous ringclosing metathesis in compressed carbondioxide

#38
20060135623
2006-06-22

Decrease in oxidative stress status through the administration of natural products and pharmaceutical drugs

#39
20050107626
2005-05-19

Alkylidene complexes of ruthenium containing N-heterocyclic carbene ligands; use as highly active, selective catalysts for olefin metathesis

#40
20050013150
2005-01-20

Alkylidene complexes of ruthenium containing N-heterocyclic carbene ligands; use as highly active, selective catalysts for olefin metathesis