Antioxidant BHT 264
CAS:128-37-0
Purity:99%
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Product Details
Synthesis Reference(s) |
Synthesis, p. 470, 1996 DOI: 10.1055/s-1996-4246 |
Purification Methods |
Distil 2-naphthaldehyde with steam then crystallise it from water or EtOH. [Beilstein 7 IV 1288.] |
Definition |
ChEBI: A naphthaldehyde that is naphthalene substituted by a formyl group at position 2. |
InChI:InChI=1/C11H8O/c12-8-9-5-6-10-3-1-2-4-11(10)7-9/h1-8H
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17β-acetoxyandrost-2-en-3-yl 2-naphthoate
stanolone acetate
(5α,17β)-3-oxoandrost-1-en-17-yl acetate
β-naphthaldehyde
Acetic acid (5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-2-(naphthalene-2-carbonyl)-3-oxo-hexadecahydro-cyclopenta[a]phenanthren-17-yl ester
Conditions | Yield |
---|---|
In
hexane;
at 0 ℃;
Quantum yield;
Mechanism;
Product distribution;
Irradiation;
variation of wavelenght, concentration, solvent, irradiation intensity, reaction time;
|
|
In
cyclohexane;
for 2h;
Irradiation;
|
15 mg 30 mg 25 mg 250 mg |
5-(2-Naphthoyl)-5H-benzocarbazole
2,3-benzocarbazole
β-naphthaldehyde
6-(2-Naphthoyl)benzocarbazole
Conditions | Yield |
---|---|
In
cyclohexane;
at 20 ℃;
for 8h;
Irradiation;
|
3.5 % Chromat. 1 % Chromat. 0.7% |
2-naphthohydrazide
ethanol
hexamethylenetetramine
2-bromomethylnaphthyl bromide
(E)-1-(4-bromophenyl)-3-(naphthalen-2-yl)prop-2-en-1-one
2-(2-nitrovinyl)naphthalene
(E)-3-(2-naphthyl)-2-propenal
4-(2-naphthylidene)-2-phenyl-5(4H)oxazolone