(S)-2-methylbutyric acid (Q27117932)

From Wikidata

Jump to navigation Jump to search

chemical compound

(S)-2-methylbutanoic acid
(S)-alpha-methylbutanoic acid
Butyric acid, 2-methyl-, L- (6CI)
(2S)-2-Methylbutanoic acid
(+)-alpha-Methylbutyric acid
(S)-(+)-2-Methylbutyric acid
Butyric acid, 2-methyl-, (S)- (8CI)
(+)-2-Methylbutyric acid
2-Methyl-(2S)-Butanoic acid
(S)-2-Methylbutyric acid
(+)-(S)-2-Methylbutanoic acid
S-(+)-2-Methylbutanoic acid
2-Methyl-(S)-Butanoic acid
(+)-2-Methylbutanoic acid

Language	Label	Description	Also known as
English	(S)-2-methylbutyric acid	chemical compound	(S)-2-methylbutanoic acid (S)-alpha-methylbutanoic acid Butyric acid, 2-methyl-, L- (6CI) (2S)-2-Methylbutanoic acid (+)-alpha-Methylbutyric acid (S)-(+)-2-Methylbutyric acid Butyric acid, 2-methyl-, (S)- (8CI) (+)-2-Methylbutyric acid 2-Methyl-(2S)-Butanoic acid (S)-2-Methylbutyric acid (+)-(S)-2-Methylbutanoic acid S-(+)-2-Methylbutanoic acid 2-Methyl-(S)-Butanoic acid (+)-2-Methylbutanoic acid

Statements

type of chemical entity

0 references

2-methylbutyric acid

1 reference

based on heuristic

inferred from SMILES

chemical structure

(S)-2-Methylbutanoic acid.svg
315 × 225; 4 KB

0 references

102.068±0 dalton

1 reference

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

(S)-2-methylbutanoate

0 references

stereoisomer of

(R)-2-methylbutyric acid

1 reference

based on heuristic

inferred from InChI

chemical formula

C₅H₁₀O₂

1 reference

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

canonical SMILES

CCC(C)C(=O)O

1 reference

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

isomeric SMILES

CC[C@H](C)C(=O)O

1 reference

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

Lithospermum erythrorhizon

1 reference

Cyclooxygenase-2 inhibitory effects and composition of the volatile oil from the dried roots of Lithospermum erythrorhizon

1 reference

The human saliva metabolome

Ipomoea capillacea

1 reference

Resin glycosides. II. Identification and characterization of the component organic and glycosidic acids of the crude resin glycoside from the seeds of Ipomoea muricata.

Ipomoea muricata

1 reference

Resin glycosides. II. Identification and characterization of the component organic and glycosidic acids of the crude resin glycoside from the seeds of Ipomoea muricata.

Mangifera indica

1 reference

Volatile components from mango (Mangifera indica L.) cultivars

1 reference

Potent odorants characterize the aroma quality of leaves and stalks in raw and boiled celery.

Humulus lupulus

1 reference

Characterization of Key Aroma Compounds in Pellets of Different Hop Varieties (Humulus lupulus L.) by Means of the Sensomics Approach

Punica granatum

1 reference

Exploitation of the health-promoting and sensory properties of organic pomegranate (Punica granatum L.) juice through lactic acid fermentation

Nicotiana tabacum

2 references

Comparison of different extraction methods: steam distillation, simultaneous distillation and extraction and headspace co-distillation, used for the analysis of the volatile components in aged flue-cured tobacco leaves

Toxicological evaluation of aerosols of a tobacco extract formulation and nicotine formulation in acute and short-term inhalation studies.

Identifiers

InChI=1S/C5H10O2/c1-3-4(2)5(6)7/h4H,3H2,1-2H3,(H,6,7)/t4-/m0/s1

1 reference

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

WLAMNBDJUVNPJU-BYPYZUCNSA-N

2 references

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

(S)-2-methylbutyric acid (English)

19 October 2016

WLAMNBDJUVNPJU-BYPYZUCNSA-N

CAS Common Chemistry

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=1730-91-2

1 reference

language of work or name

(S)-2-METHYLBUTYRIC ACID (English)

19 October 2016

1 reference

language of work or name

(S)-(+)-2-Methylbutyric acid (English)

19 October 2016

Reaxys registry number

3648078

1 reference

language of work or name

(S)-2-methylbutyric acid (English)

19 October 2016

1720485

1 reference

language of work or name

(S)-2-methylbutyric acid (English)

19 October 2016

532948

0 references

mapping relation type

1 reference

language of work or name

(S)-2-methylbutyric acid (English)

19 October 2016

1 reference

language of work or name

CHEMBL1162482 (English)

19 October 2016

UniChem compound ID

1 reference

DSSTox substance ID

0 references

DSSTOX compound identifier

DTXCID501022529

0 references

605-661-4

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

(S)-(+)-2-Methylbutyric acid (English)

CAS no.: 1730-91-2 (English)

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

(S)-(+)-2-Methylbutyric acid (English)

CAS no.: 1730-91-2 (English)

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

WLAMNBDJUVNPJU-BYPYZUCNSA-N

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

WLAMNBDJUVNPJU-BYPYZUCNSA-N

1 reference

Global Substance Registration System

language of work or name

(S)-2-methylbutyric acid (English)

19 October 2016

0 references

PDB structure ID

1 reference

Protein Data Bank

PDB structure ID

language of work or name

1YA8 (English)

19 October 2016

1 reference

Protein Data Bank

PDB structure ID

language of work or name

1UKA (English)

19 October 2016

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q27117932&oldid=2153274775"