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Chemical Structure| 36338-96-2 Chemical Structure| 36338-96-2
Chemical Structure| 36338-96-2

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Safflower yellow is the main active component in the traditional Chinese medicine safflower, modulates inflammatory responses by acting directly on BV2 microglia.

Synonyms: Safflower Red; Carthamin Yellow; Liofresh Red CR

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Product Details of SAFFLOWER YELLOW

CAS No. :36338-96-2
Formula : C43H42O22
M.W : 910.78
SMILES Code : O[C@](C(O)=C(C(/C=C/C1=CC=C(O)C=C1)=O)C2=O)([C@]([C@@H]([C@@H](O)[C@@H]3O)O)([H])O[C@@H]3CO)C(/C2=C\C(C(C(C(/C=C/C4=CC=C(O)C=C4)=O)=C5O)=O)=C([C@]5([C@]([C@@H]([C@@H](O)[C@@H]6O)O)([H])O[C@@H]6CO)O)O)=O
Synonyms :
Safflower Red; Carthamin Yellow; Liofresh Red CR
MDL No. :MFCD09954647
InChI Key :WLYGSPLCNKYESI-RSUQVHIMSA-N
Pubchem ID :135565560

Safety of SAFFLOWER YELLOW

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338
 

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Technical Information

• Appel Reaction • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Chugaev Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Kim Oxidation • Dess-Martin Oxidation • Fischer Indole Synthesis • Grignard Reaction • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Jones Oxidation • Lawesson's Reagent • Leuckart-Wallach Reaction • Martin's Sulfurane Dehydrating Reagent • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mitsunobu Reaction • Moffatt Oxidation • Oxidation of Alcohols by DMSO • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Alcohols • Preparation of Aldehydes and Ketones • Preparation of Amines • Prins Reaction • Reactions of Alcohols • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions with Organometallic Reagents • Reformatsky Reaction • Ritter Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Ketenes • Stobbe Condensation • Swern Oxidation • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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