(Q22984229)

2-Methylanthraquinone (English)

5 October 2016

chemical formula

C₁₅H₁₀O₂

1 reference

2-Methylanthraquinone (English)

5 October 2016

canonical SMILES

CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O

1 reference

2-Methylanthraquinone (English)

5 October 2016

melting point

172.0 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Handroanthus impetiginosum

2 references

High-performance liquid chromatographic separation of some naturally occurring naphtoquinones and anthraquinones

Naturally occurring quinones. Part X. The quinonoid constituents of Tabebuia avellanedae(Bignoniaceae)

Tectona grandis

3 references

A 1,4-Anthraquinone derivative from Tectona grandis

Activity of quinones from teak (Tectona grandis) on fungal cell wall stress.

Chemical components of the roots of Tectona grandis and Gmelina arborea

Rubia oncotricha

1 reference

Anthraquinones, naphthoquinones and naphthohydroquinones from Rubia oncotricha

Rubia cordifolia

2 references

Two naphthoquinones from Rubia cordifolia

Preparative separation of anti-oxidative constituents from Rubia cordifolia by column-switching counter-current chromatography

Barbados nut

1 reference

New lathyrane and podocarpane diterpenoids from Jatropha curcas

Lippia origanoides

2 references

Chemical constituents from Lippia sidoides and cytotoxic activity

[Chemical constituents from Pteris multifida and cytotoxic activity].

Lippia sidoides

2 references

Chemical constituents from Lippia sidoides and cytotoxic activity

[Chemical constituents from Pteris multifida and cytotoxic activity].

Lygodium flexuosum

1 reference

A new triterpene ester, an anthraquinone and other constituents of the fern Lygodium flexuosum

Newbouldia laevis

2 references

Newbouldiaquinone A: A naphthoquinone-anthraquinone ether coupled pigment, as a potential antimicrobial and antimalarial agent from Newbouldia laevis

Newbouldiaquinone and newbouldiamide: a new naphthoquinone-anthraquinone coupled pigment and a new ceramide from Newbouldia laevis

Tecomella undulata

2 references

A New Ferulic Ester fromTecomella undulata

6-O-veratryl catalposide: A new iridoid glucoside from Tecomella undulata

Diospyros sylvatica

2 references

Antitermitic Quinones from Diospyros sylvatica

Antitermitic quinones from Diospyros sylvatica

Morinda lucida

1 reference

Antifungal anthraquinones from Morinda lucida

Ophiorrhiza pumila

1 reference

Anthraquinones from Ophiorrhiza pumila tissue and cell cultures

Dolichopentas longiflora

1 reference

New pyranonaphthoquinone and pyranonaphthohydroquinone from the roots of Pentas longiflora

Rhinacanthus nasutus

1 reference

A quinol and steroids from the leaves and stems of Rhinacanthus nasutus

Rubia tinctorum

1 reference

The mutagenic constituents of Rubia tinctorum

Diospyros maritima

1 reference

Synergistic TRAIL sensitizers from Barleria alluaudii and Diospyros maritima

Camellia sinensis

1 reference

Effect of green tea (Camellia sinensis) extract on the rat diaphragm

Clausena heptaphylla

1 reference

2-Methylanthraquinone from Clausena heptaphylla

Plocama pendula

1 reference

Anthraquinones from natural and transformed roots of Plocama pendula

Rubia yunnanensis

1 reference

Constituents fromRubia UstulataDiels andR. YunnanensisDiels and Their Antiplatelet Aggregation Activity

Sinningia aggregata

1 reference

Lactones and quinones from the tubers of Sinningia aggregata.

Barleria alluaudii

1 reference

Synergistic TRAIL sensitizers from Barleria alluaudii and Diospyros maritima

Handroanthus impetiginosus

2 references

Naturally occurring quinones. Part X. The quinonoid constituents of Tabebuia avellanedae(Bignoniaceae)

High-performance liquid chromatographic separation of some naturally occurring naphtoquinones and anthraquinones

Gynochthodes officinalis

1 reference

Chemical constituents of Chinese natural medicine, morindae radix, the dried roots of morinda officinalis how.: structures of morindolide and morofficinaloside

Identifiers

InChI

InChI=1S/C15H10O2/c1-9-6-7-12-13(8-9)15(17)11-5-3-2-4-10(11)14(12)16/h2-8H,1H3

1 reference

2-Methylanthraquinone (English)

NJWGQARXZDRHCD-UHFFFAOYSA-N

5 October 2016

InChIKey

2 references

2-Methylanthraquinone (English)

5 October 2016

ChEBI release 2020-09-01

2 references

https://commonchemistry.cas.org/detail?cas_rn=84-54-8

2-methylanthraquinone (English)

5 October 2016

7 April 2021

InChIKey

NJWGQARXZDRHCD-UHFFFAOYSA-N

1 reference

2-Methylanthraquinone (English)

5 October 2016

1 reference

2-Methylanthraquinone (English)

5 October 2016

Reaxys registry number

2050523

1 reference

2-methylanthraquinone (English)

5 October 2016

Gmelin number

1607902

0 references

ChEBI ID

9427

mapping relation type

1 reference

2-methylanthraquinone (English)

5 October 2016

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

TECTOQUINONE (English)

5 October 2016

1 reference

1 reference

DSSTOX compound identifier

0 references

0 references

201-539-6

1 reference

Global Substance Registration System

UNII

Q9P233HWAJ

2-METHYLANTHRAQUINONE (English)

ECHA Substance Infocard ID

5 October 2016

100.001.399

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.001.399

27 December 2018

PesticideInfo chemical ID

2-methylanthraquinone (English)

quotation

CAS no.: 84-54-8 (English)

PRI317

0 references

AICS Chemical ID (BEING DELETED)

0 references

2 references

2-methylanthraquinone (English)

5 October 2016

based on heuristic

inferred from InChIKey

UNII

Q9P233HWAJ

1 reference

Global Substance Registration System

UNII

Q9P233HWAJ

2-METHYLANTHRAQUINONE (English)

5 October 2016

0 references

1 reference

2-methylanthraquinone (English)