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DULCITOL

CAS No.6051-87-2
Chemical Name:DULCITOL
Synonyms:BNF;BETA-NF;DULCITE;MELAMPYRITE;β-Naphthoflavon;5,6-BENZOFLAVONE;B-NAPHTHOFLAVONE;BetaNapthoflavone;SS-NAPHTHOFLAVONE;B-NAPHTHOFLAVANONE
CBNumber:CB7174209
Molecular Formula:C19H12O2
Formula Weight:272.3
MOL File:6051-87-2.mol
DULCITOL Property
mp : 185-189 °C
bp : 275-280 °C (1 mmHg)
storage temp. : 2-8°C
color : yellow to tan
BRN : 18991
CAS DataBase Reference: 6051-87-2(CAS DataBase Reference)
Safety
Hazard Codes : Xn,Xi,C,F
Risk Statements : 22-34-11
Safety Statements : 24/25-45-36/37/39-26-16
WGK Germany : 3
RTECS : QL6200000
F : 3-10
Hazard Note : Irritant

DULCITOL Chemical Properties,Usage,Production

Chemical Properties
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DULCITOL Preparation Products And Raw materials
Raw materials
Preparation Products
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6051-87-2(DULCITOL)Related Search:
Dulcitol 4'-METHOXY-5,6-BENZOFLAVONE 2-IODO-3-PHENYL-1H-NAPHTHO[2,1-B]PYRAN-1-ONE 4'-HYDROXY-BETA-NAPHTHOFLAVONE 2'-HYDROXY-BETA-NAPHTHOFLAVONE 2'-METHOXY-BETA-NAPHTHOFLAVONE 3'-METHOXY-BETA-NAPHTHOFLAVONE 3',4'-DIMETHOXY-BETA-NAPHTHOFLAVONE DULCITOL 3',4'-DIHYDROXY-BETA-NAPHTHOFLAVONE 3'-HYDROXY-B-NAPHTHOFLAVONE BETA-NAPHTHOFLAVANOL
Sugar Alcohols Galactose Sugars 1-b)pyran-1-one,3-phenyl-1h-naphtho( 1H-Naphtho[2,1-b]pyran-1-one,3-phenyl- 3-Phenyl-1H-benzo[f]chromen-1-one 3-Phenyl-1H-naphtho(2,1-b)pyran-1-one 3-Phenyl-1H-naphtho[2,1-b]pyran-1-one 3-Phenyl-benzo[f]chromen-1-one β-Naphthoflavon 5,6-BENZOFLAVONE 6051-87-2 Building Blocks BioChemical Benzopyrans Cancer Research Chemopreventive Agents MELAMPYRITE BNF B-NAPHTHOFLAVANONE B-NAPHTHOFLAVONE BETA-NAPHTHOFLAVONE BETA-NF DULCITE NAPHTHOFLAVANONE, B- NAPHTHOFLAVONE, B- Heterocyclic Building Blocks Phase I Enzyme Inducer BETA-NAPHTHOFLAVONE, 98+% BetaNapthoflavone ~-Naphthoflavone,98% beta-Naphthoflavone, 99+% C19H12O2 C6H8OH6 NAPHTHO(2,1-B)PYRAN-1-ONE,3-PHENYL- SS-NAPHTHOFLAVONE Flavones 6051-59-1 ^b-Naphthoflavone, 98+% beta-Naphthoflavone, 99+% 1GR Phase I Enzyme Inducer Phase I Enzyme Inducers Benzopyrans Bioactive Small Molecules Building Blocks Cancer Research Cell Biology Chemical Synthesis Chemopreventive Agents Heterocyclic Building Blocks Multidrug Resistance N
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