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(Q105303631)
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English
(2R)-2-methyl-2-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanenitrile
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
(2RS)-Lotaustralin
1 reference
based on heuristic
inferred from SMILES
2(R)-Hydroxy-2-methylbutyronitrile-beta-D-glucopyranoside
1 reference
based on heuristic
inferred from SMILES
mass
261.121237328
dalton
1 reference
based on heuristic
inferred from SMILES
stereoisomer of
lotaustralin
2 references
based on heuristic
inferred from InChIKey
based on heuristic
inferred from InChI
2-(Hexopyranosyloxy)-2-methylbutanenitrile
1 reference
based on heuristic
inferred from InChI
chemical formula
C₁₁H₁₉NO₆
0 references
canonical SMILES
N#CC(OC1OC(CO)C(O)C(O)C1O)(C)CC
0 references
isomeric SMILES
CC[C@](C)(C#N)O[C@@H]1O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
0 references
found in taxon
Acacia aroma
1 reference
stated in
Cyanogenic Glycosides from Four Latin American Species of Acacia
Passiflora adenopoda
1 reference
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
Passiflora lutea
1 reference
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
Passiflora morifolia
1 reference
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
Passiflora pendens
1 reference
stated in
Cyanohydrin glycosides of Passiflora: distribution pattern, a saturated cyclopentane derivative from P. guatemalensis, and formation of pseudocyanogenic alpha-hydroxyamides as isolation artefacts
Rhodiola rosea
1 reference
stated in
Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis
Rhodiola sachalinensis
1 reference
stated in
Bioactive constituents from Chinese natural medicines. XXVI. Chemical structures and hepatoprotective effects of constituents from roots of Rhodiola sachalinensis
Vachellia aroma
1 reference
stated in
Cyanogenic Glycosides from Four Latin American Species of Acacia
Identifiers
InChI
InChI=1S/C11H19NO6/c1-3-11(2,5-12)18-10-9(16)8(15)7(14)6(4-13)17-10/h6-10,13-16H,3-4H2,1-2H3/t6-,7+,8-,9-,10-,11+/m0/s1
0 references
InChIKey
WEWBWVMTOYUPHH-HQPKYVJOSA-N
0 references
PubChem CID
154496924
2 references
stated in
PubChem
retrieved
17 September 2022
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
WEWBWVMTOYUPHH-HQPKYVJOSA-N
UniChem compound ID
185783830
1 reference
stated in
UniChem
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