(-)-epicatechin pentaacetate
tetrachloromethane
N-Bromosuccinimide
dibenzoyl peroxide
cyanidin chloride
Conditions | Yield |
---|---|
Erwaermen mit Chlorwasserstoff enthaltendem Aethanol oder mit wss. Natriumacetat-Loesung und Zinkchlorid in Cyanidin-chlorid; |
Conditions | Yield |
---|---|
With hydrogenchloride; magnesium at 35℃; | |
With hydrogenchloride; sodium amalgam |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogen iodide; phenol Umsetzen des entstandenen Jodids mit Silberchlorid und Salzsaeure; |
(2R,3S)-(+)-catechin 3',4',5,7-tetramethyl ether
cyanidin chloride
Conditions | Yield |
---|---|
With 1,4-dioxane; bromine Erwaermen des jeweiligen Reaktionsprodukts mit wss. Jodwasserstoffsaeure, Phenol und Phosphor unter Kohlendioxid; Behandeln des erhaltenen Jodids mit Silberchlorid in wss.-aethanol. Salzsaeure; |
(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol
A
cyanidin chloride
B
fisetinidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride In isopropyl alcohol at 97℃; |
(2S,3S,4S)-4-(2,4-Dihydroxy-phenyl)-2-(3,4-dihydroxy-phenyl)-chroman-3,5,7-triol
A
cyanidin chloride
B
fisetinidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride In isopropyl alcohol at 97℃; |
hydrogenchloride
2,3,5,7-tetraacetoxy-2-(3,4-diacetoxy-phenyl)-2H-chromene
acetic acid
cyanidin chloride
Conditions | Yield |
---|---|
at 35℃; |
cyanidin chloride
Conditions | Yield |
---|---|
With tetrachloromethane; N-Bromosuccinimide; dibenzoyl peroxide Erwaermen des Reaktionsprodukts mit Chlorwasserstoff enthaltendem Aethanol oder mit wss. Natriumacetat-Loesung und Zinkchlorid; |
cyanidin chloride
Conditions | Yield |
---|---|
With 1,4-dioxane; bromine Erwaermen des jeweiligen Reaktionsprodukts mit wss. Jodwasserstoffsaeure, Phenol und Phosphor unter Kohlendioxid; Behandeln des erhaltenen Jodids mit Silberchlorid in wss.-aethanol. Salzsaeure; |
1,3,5-triacetoxy-2-diacetoxymethyl-benzene
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride; acetic acid Kochen des Reaktionsprodukts mit Salzsaeure; |
cyanidin chloride
Conditions | Yield |
---|---|
With sodium hydroxide Erwaermen des Reaktionsgemisches mit Salzsaeure auf 60grad; |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogen iodide; phenol Umsetzen des entstandenen Jodids mit Silberchlorid und Salzsaeure; |
cyanidin chloride
Conditions | Yield |
---|---|
With fermenting yeast | |
With hydrogenchloride | |
With aspergillus-tannase |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride |
(2R,3S,4S)-2,3-trans-3,4-trans-4-(2,4,6-trihydroxyphenyl)flavan-3,3',4',7-tetraol
cyanidin chloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 30 mg / 0.05M benzophenone / acetone / Irradiation 2: 3M HCl / propan-2-ol / 97 °C View Scheme |
Conditions | Yield |
---|---|
Acidic conditions; |
A
D-Glucose
B
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
C
malonic acid
D
p-Coumaric Acid
E
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride; water at 100℃; for 1h; |
acetic anhydride
cyanidin chloride
A
1,3,5-triacetoxybenzene
B
3,4-Diacetoxy-benzoesaeure
Conditions | Yield |
---|---|
With ruthenium(IV) oxide; sodium periodate 1) 5 h, room temp., pyridine; 2) acetone, water, 20 min : decomposition reaction; | A 32% B 67% |
With ruthenium(IV) oxide; sodium periodate 1) 5 h, room temp., pyridine; 2) water, acetone, 20 min; Yield given. Multistep reaction. Yields of byproduct given; |
acetic anhydride
cyanidin chloride
2,3,5,7-tetraacetoxy-2-(3,4-diacetoxy-phenyl)-2H-chromene
Conditions | Yield |
---|---|
With pyridine |
cyanidin chloride
2-(3,4-dihydroxy-phenyl)-3,5,7-trihydroxy-chromenylium; benzopyrylium hydroxide
Conditions | Yield |
---|---|
With ethanol; water |
cyanidin chloride
Conditions | Yield |
---|---|
With hydrogenchloride; methanol; platinum Hydrogenation; |
Conditions | Yield |
---|---|
at 210 - 250℃; |
Conditions | Yield |
---|---|
Hydration; |
Molecular Formula:C15H11ClO6
Formula Weight:322.7g/mol
storage temp.:-20°C
EINECS:208-438-6
Product Categories: Anthocyanins;Flavonoids
Product Categories of Cyanidin chloride (528-58-5): Anthocyanins; Flavonoids
Structure of Cyanidin chloride (528-58-5):
It can be used as food pigment, cosmetics, etc.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Source |
---|---|---|---|---|
dog | LD | oral | > 3gm/kg (3000mg/kg) | Drugs of the Future. Vol. 14, Pg. 224, 1989. |
mammal (species unspecified) | LD | oral | > 6gm/kg (6000mg/kg) | Drugs of the Future. Vol. 14, Pg. 224, 1989. |
rat | LD50 | intraperitoneal | 1500mg/kg (1500mg/kg) | United States Patent Document. Vol. #4229439, |
Safety Statements: 22-24/25
S22: Do not breathe dust
S24/25: Avoid contact with skin and eyes
WGK Germany: 3
RTECS: LK9824000
F: 10-21
F 10: Keep under argon
F 21: Sensitive to humidity
Cyanidin chloride (CAS NO.528-58-5) is also called as 1-Benzopyrylium, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride ; 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-benzopyrylium chloride ; 3,3',4',5,7-Pentahydroxy-2-phenylbenzopyrylium chloride ; 3,3'4',5,7-Pentahydroxyflavylium chloride ; Cyanidin chloride ; Cyanidol chloride ; Gastrotelos ; 1-Benzopyrylium, 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-, chloride (9CI) ; 3,3',4',5,7-Pentahydroxyflavylium chloride Flavylium, 3,3'4',5,7-pentahydroxy-, chloride
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