:Neohesperidose

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| Verifiedfields = changed

| Watchedfields = changed

| verifiedrevid = 415344475

| Name = Neohesperidose

| ImageFile = Neohesperidose.svg

| ImageFile2 = Neohesperidose 3D BS.png

| IUPACName = α-L-Rhamnopyranosyl-(1→2)-D-glucose

| SystematicName = (2R,3S,4R,5R)-3,4,5,6-Tetrahydroxy-2-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}hexanal

| OtherNames = 2-O-alpha-L-Rhamnopyranosyl-D-glucopyranose
2-O-alpha-L-Rhamnosyl-D-glucose
2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranose

|Section1={{Chembox Identifiers

| CASNo_Ref = {{cascite|correct|??}}

| CASNo = 17074-02-1

| PubChem = 441426

| EINECS =

| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID = 390159

| ChEBI_Ref = {{ebicite|changed|EBI}}

| ChEBI = 73992

| ChEMBL_Ref = {{ebicite|changed|EBI}}

| ChEMBL = 1651520

| KEGG_Ref = {{keggcite|changed|kegg}}

| KEGG = C08244

| SMILES = O([C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O)[C@@H]2O[C@H]([C@H](O)[C@@H](O)[C@H]2O)C

| InChI = 1/C12H22O10/c1-3-5(14)7(16)9(18)12(20-3)22-10-8(17)6(15)4(2-13)21-11(10)19/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12-/m0/s1

| InChIKey = VSRVRBXGIRFARR-OUEGHFHCBJ

| StdInChI_Ref = {{stdinchicite|changed|chemspider}}

| StdInChI = 1S/C12H22O10/c1-3-5(14)7(16)9(18)12(20-3)22-10-8(17)6(15)4(2-13)21-11(10)19/h3-19H,2H2,1H3/t3-,4+,5-,6+,7+,8-,9+,10+,11+,12-/m0/s1

| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}

| StdInChIKey = VSRVRBXGIRFARR-OUEGHFHCSA-N

}}

|Section2={{Chembox Properties

| Formula = C12H22O10

| MolarMass = 326.29 g/mol

| Appearance =

| Density = 1.662 g/mL

| MeltingPt =

| BoilingPt =

| Solubility =

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|Section3={{Chembox Hazards

| MainHazards =

| FlashPt =

| AutoignitionPt =

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| Section8 = {{Chembox Related

| OtherCompounds = Rhamnose
Glucose

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Neohesperidose is the disaccharide which is present in some flavonoids. It can be found in species of Typha.{{cite journal | url=https://www.sciencedirect.com/science/article/abs/pii/S0040402001992117 | doi=10.1016/S0040-4020(01)99211-7 | title=Flavonoids of citrus—VI: The structure of neohesperidose | journal=Tetrahedron | date=January 1963 | volume=19 | issue=5 | pages=773–782 | last1=Horowitz | first1=R. M. | last2=Gentili | first2=Bruno | url-access=subscription }}{{Cite journal |doi=10.1016/0031-9422(89)80039-1 |title=Delphinidin-3-neohesperidoside and cyanidin-3- neohesperidoside from receptacles of Podocarpus species |date=1989 |last1=Andersen |first1=Oyvind M. |journal=Phytochemistry |volume=28 |issue=2 |pages=495–497 |bibcode=1989PChem..28..495A }}

Neohesperidosides

See also

References

  • [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6THR-436X607-4&_user=10&_coverDate=12%2F31%2F1968&_alid=989895831&_rdoc=2&_fmt=high&_orig=search&_cdi=5289&_docanchor=&view=c&_ct=101&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=4c2b6cd1646e71ebf0b420f1abe696a6 Synthesis of neohesperidose, B. H. Koeppen, 1968]{{dead link|date=January 2025|bot=medic}}{{cbignore|bot=medic}}

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