CARVONE, (±)-

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NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C10H14O
Molecular Weight	150.2176
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of CARVONE, (±)-

Structure Search

SMILES

CC(=C)C1CC=C(C)C(=O)C1

InChI

InChIKey=ULDHMXUKGWMISQ-UHFFFAOYSA-N

InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3

HIDE SMILES / InChI

Molecular Formula	C10H14O
Molecular Weight	150.2176
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:01:13 UTC 2023` Edited by `admin` on `Fri Dec 15 17:01:13 UTC 2023`
Record UNII	75GK9XIA8I
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CARVONE, (±)-

Common Name

English

CARVONE, (+-)-

Common Name

English

5-ISOPROPYL-2-METHYL-2-CYCLOHEXEN-1-ONE

Systematic Name

English

CARVONE [ISO]

Common Name

English

CARVONE [HSDB]

Common Name

English

NSC-6275

Code

English

CARVONE

Official Name

English

2-METHYL-5-ISOPROPENYL-2-CYCLOHEXENONE

Systematic Name

English

CARVONE, DL-

Common Name

English

P-MENTHA-1(6),8-DIEN-2-ONE

Systematic Name

English

DL-CARVONE

Common Name

English

CARVONE [MI]

Common Name

English

LIMONEN-6-ONE

Common Name

English

CARVONE DL-FORM [MI]

Common Name

English

CARVONE [INCI]

Common Name

English

(±)-CARVONE

Common Name

English

P-MENTHA-6,8-DIEN-2-ONE

Common Name

English

(RS)-5-ISOPROPENYL-2-METHYLCYCLOHEX-2-EN-1-ONE

Systematic Name

English

2-METHYL-5-(1-METHYLETHENYL)-2-CYCLOHEXENE-1-ONE

Systematic Name

English

2-METHYL-5-(1-METHYLETHENYL)-2-CYCLOHEXEN-1-ONE

Systematic Name

English

FEMA NO. 2249, (±)-

Code

English

KARVON

Common Name

English

Code System Code Type Description

ECHA (EC/EINECS)

202-759-5

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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WIKIPEDIA

Carvone

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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MERCK INDEX

m3144

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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Merck Index

MERCK INDEX

m3144

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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Merck Index

NSC

6275

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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EPA CompTox

DTXSID8047426

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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CAS

99-49-0

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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PUBCHEM

7439

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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HSDB

707

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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RXCUI

1427075

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

ALTERNATIVE

DAILYMED

75GK9XIA8I

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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EVMPD

SUB127035

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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ALANWOOD

carvone

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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RXCUI

1427074

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

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FDA UNII

75GK9XIA8I

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

PRIMARY

CHEBI

38265

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

PRIMARY

SMS_ID

100000153169

Created by admin on Fri Dec 15 17:01:13 UTC 2023 , Edited by admin on Fri Dec 15 17:01:13 UTC 2023

PRIMARY

Related Record Type Details


					3IXW0F6P8W

ELYMUS REPENS ROOT

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

Compound measured as 5.50% of the composition of the steam distillate of Elymus repens rhizome as per R Boesel in Planta Medica iss:4 pg:399-400, 1989.

Amount: