Rubrocurcumin: Difference between revisions

Rubrocurcumin
Names
	Other names Rubrocurcumin
Identifiers
CAS Number	12098-66-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	24751750 Non-charged form ; 24751749 Charged form ;
CompTox Dashboard (EPA)	DTXSID90726681 ;
	InChI InChI=1S/C23H19BO10/c1-30-20-11-14(5-9-18(20)26)3-7-16(25)13-17(32-24-33-22(28)23(29)34-24)8-4-15-6-10-19(27)21(12-15)31-2/h3-13,26-27H,1-2H3/b7-3+,8-4+,17-13- Key: CSMMVHRUFPYHCS-YRLHZMKXSA-N ; Charged form: InChI=1S/C23H19BO10/c1-29-20-11-14(5-9-18(20)25)3-7-16-13-17(32-24(31-16)33-22(27)23(28)34-24)8-4-15-6-10-19(26)21(12-15)30-2/h3-13,25-26H,1-2H3/b7-3+,8-4+ Key: YIFZXJZUXMHJJG-FCXRPNKRSA-N;
	SMILES B1(OC(=O)C(=O)O1)O/C(=C\C(=O)/C=C/c2ccc(c(c2)OC)O)/C=C/c3ccc(c(c3)OC)O;
Properties
Chemical formula	C23H19BO10
Molar mass	466.19 g/mol
Appearance	red solid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

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Revision as of 21:28, 6 March 2019

Rubrocurcumin is a red-colored dye that is formed by the reaction of curcumin and borates.

Synthesis

The reaction of curcumin with borates in presence of oxalic acid produces rubrocurcumin.^[1]

Characteristics

Rubrocurcumin produces a red colored solution.

Rubrocurcumin is a neutrally charged composition, while rosocyanine is produced from ions. In rubrocurcumin, one molecule of curcumin is replaced with oxalate compared to rosocyanine.

Complexes with boron such as rubrocurcumin are called 1,3,2-dioxaborines.^[1]

References

^ ^a ^b Rohde, D. (2002). Darstellung und Eigenschaftsuntersuchungen an 1,3,2-Dioxaborinen mit variablen Coliganden am Boratom [Presentation and characterization of 1,3,2-dioxaborins with variable coligands on the boron atom] (Dissertation). University Halle.

@@ Line 45: / Line 45: @@
 == Synthesis ==
-The reaction of curcumin with borates in presence of [[oxalic acid]] produces rubrocurcumin.<ref name="rohde">{{ cite web | author = Rohde, D. | url = http://sundoc.bibliothek.uni-halle.de/diss-online/02/02H082/ | title = Darstellung und Eigenschaftsuntersuchungen an 1,3,2-Dioxaborinen mit variablen Coliganden am Boratom (Dissertation) | date = 2002 | publisher = University Halle }}</ref>
+The reaction of curcumin with borates in presence of [[oxalic acid]] produces rubrocurcumin.<ref name="rohde">{{ cite thesis| last = Rohde|first= D. | url = http://sundoc.bibliothek.uni-halle.de/diss-online/02/02H082/ | title = Darstellung und Eigenschaftsuntersuchungen an 1,3,2-Dioxaborinen mit variablen Coliganden am Boratom |trans-title= Presentation and characterization of 1,3,2-dioxaborins with variable coligands on the boron atom |type=Dissertation | date = 2002 | publisher = University Halle }}</ref>
 == Characteristics ==
@@ Line 53: / Line 53: @@
 [[Complex (chemistry)|Complexes]] with [[boron]] such as rubrocurcumin are called 1,3,2-dioxaborines.<ref name="rohde" />
-== Literature ==
-* {{ cite journal | author = Spicer, G. S.| author2 = Strickland, J. D. H. | title = Compounds of Curcumin and Boric Acid. Part II. The Structure of Rubrocurcumin | journal = Journal of the Chemical Society | location = London | date = 1952 | volume = 1952 | issue = article 907 | pages = 4650–4653 | doi = 10.1039/JR9520004650 }}
 == References ==
 {{reflist}}
+=== Further reading ===
+{{refbegin}}
+* {{ cite journal | last = Spicer | first = G. S. | last2 = Strickland | first2 = J. D. H. | title = Compounds of Curcumin and Boric Acid. Part II. The Structure of Rubrocurcumin | journal = Journal of the Chemical Society | location = London | date = 1952 | volume = 1952 | issue = art. 907 | pages = 4650–4653 | doi = 10.1039/JR9520004650 }}
+{{refend}}
 [[Category:Curcuminoid dyes]]
 [[Category:Borates]]