Details
Quality products?make an important contribution to long-term revenue and profitability. Factory supply 2-Bromo-1-tetralone 13672-07-6 with sufficient production capacity
1.What is the 2-Bromo-1-tetralone ?
Used in Pharmaceutical Industry:
2-Bromo-1-tetralone is used as a key intermediate for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
2-Bromo-1-tetralone is utilized as a building block in the synthesis of a wide range of organic compounds. Its reactivity and functional group compatibility make it a valuable component in the creation of complex organic molecules for various applications.
Used in Laboratory Research:
In the field of laboratory research, 2-Bromo-1-tetralone is employed as a versatile compound for exploring new chemical reactions and synthetic pathways. Its properties enable researchers to investigate novel methods for the synthesis of pharmaceuticals and other organic compounds.
Used in Commercial Production:
2-Bromo-1-tetralone is also used in commercial production processes, where it serves as a crucial component in the manufacturing of various pharmaceuticals and organic compounds. Its widespread use in the industry highlights its importance in the development of new and innovative products.
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51114-70-6
2,2-dibromo-1,2,3,4-tetrahydronaphthalen-1-one
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1056246-70-8,13672-07-6
2-bromo-1-tetralone
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529-34-0
3,4-dihydronaphthalene-1(2H)-one
| Conditions | Yield |
|---|---|
|
With
water; 1-methyl-3-pentyl-1H-imidazolium tetrafluoroborate;
at 125 ℃;
for 0.0333333h;
under 2585.74 Torr;
microwave irradiation;
|
86%
|
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529-34-0
3,4-dihydronaphthalene-1(2H)-one
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1056246-70-8,13672-07-6
2-bromo-1-tetralone
| Conditions | Yield |
|---|---|
|
With
bromine;
In
diethyl ether;
for 2h;
-10 deg C -> RT;
|
99%
|
|
With
N-Bromosuccinimide; ammonium acetate;
In
diethyl ether;
at 25 ℃;
for 1.5h;
|
99%
|
|
With
bromine;
In
diethyl ether;
Cooling with ice;
|
99%
|
|
With
Oxone; ammonium bromide;
In
methanol;
for 0.333333h;
regioselective reaction;
Reflux;
|
98%
|
|
With
sodium hydrogen sulfate; N-Bromosuccinimide; silica gel;
at 20 ℃;
for 1h;
|
97%
|
|
With
bromine;
at 0 - 20 ℃;
|
94%
|
|
With
copper(II) nitrate trihydrate; hydrogen bromide; oxygen;
at 70 ℃;
for 2h;
Green chemistry;
|
94%
|
|
With
N-Bromosuccinimide;
In
various solvent(s);
at 20 ℃;
for 0.333333h;
|
92%
|
|
With
Galden HT135; bromine; potassium carbonate;
In
chloroform;
at 20 ℃;
for 48h;
|
92%
|
|
With
bromine;
In
diethyl ether;
at 0 ℃;
for 0.583333h;
Inert atmosphere;
|
92%
|
|
With
bromine;
In
diethyl ether;
at 0 - 20 ℃;
|
91%
|
|
With
copper(ll) bromide;
In
chloroform; ethyl acetate;
for 5h;
Heating;
|
90%
|
|
With
N-Bromosuccinimide;
In
dimethyl sulfoxide;
at 20 - 65 ℃;
|
90%
|
|
With
bromine;
In
diethyl ether;
at 0 ℃;
for 2h;
|
90%
|
|
With
hydrogen bromide; dihydrogen peroxide;
In
water;
at 20 ℃;
for 24h;
Darkness;
|
88%
|
|
With
bromine;
In
diethyl ether;
at 0 ℃;
for 0.333333h;
regiospecific reaction;
Inert atmosphere;
|
88%
|
|
With
N-Bromosuccinimide; trimethylsilyl trifluoromethanesulfonate;
In
acetonitrile;
at 20 ℃;
for 24h;
|
87%
|
|
With
ammonium cerium(IV) nitrate;
at 25 - 28 ℃;
for 4h;
|
87%
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
at 20 ℃;
for 2h;
|
86%
|
|
With
trifluorormethanesulfonic acid; bromine;
In
dichloromethane;
at 20 ℃;
Inert atmosphere;
|
86%
|
|
With
N-Bromosuccinimide; urea-hydrogen peroxide; 1-butyl-3-methylimidazolium Tetrafluoroborate;
at 60 ℃;
|
85%
|
|
With
N-Bromosuccinimide; copper(II) bis(trifluoromethanesulfonate);
In
chloroform;
for 7h;
Reflux;
Inert atmosphere;
|
85%
|
|
With
N-Bromosuccinimide; tetrachlorosilane;
In
acetonitrile;
at 20 ℃;
for 7h;
|
85%
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
In
acetonitrile;
for 22h;
Reflux;
|
82%
|
|
With
triphenylphosphine hydrobromide; dimethyl sulfoxide;
at 20 ℃;
for 12h;
chemoselective reaction;
Inert atmosphere;
|
78%
|
|
With
pyridinium hydrobromide perbromide;
In
methanol;
stereoselective reaction;
Reflux;
Inert atmosphere;
|
76%
|
|
With
aluminum oxide; hexamethylenetetramine; bromine;
for 0.166667h;
microwave irradiation;
|
75%
|
|
With
hydrogen bromide; bromine; acetic acid;
at 25 ℃;
for 3h;
|
67%
|
|
With
tert.-butylhydroperoxide; hydrogen bromide;
In
1,4-dioxane; water;
for 20h;
Heating;
|
64%
|
|
With
ferric(III) bromide; [bis(acetoxy)iodo]benzene;
In
acetic acid;
at 20 ℃;
for 16h;
Inert atmosphere;
|
60%
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
at 80 ℃;
for 2h;
|
57%
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
at 80 ℃;
for 2h;
|
57%
|
|
With
tetra-N-butylammonium tribromide;
In
methanol; dichloromethane;
at 20 ℃;
|
50%
|
|
With
bromine; acetic acid;
|
|
|
With
carbon disulfide; bromine;
|
|
|
With
bromine; acetic acid;
|
|
|
With
bromine;
In
diethyl ether; chloroform;
|
|
|
With
bromine;
In
tetrachloromethane;
|
|
|
With
potassium bromide; copper(ll) bromide;
In
methanol; water;
for 4h;
Heating;
|
|
|
With
bromine complrex of poly(styrene-co-4-vinylpyridine); dibenzoyl peroxide;
In
tetrachloromethane;
for 4h;
Heating;
|
|
|
With
bromine;
In
methanol;
|
|
|
With
hydrogen bromide; bromine;
In
acetic acid;
|
|
|
With
bromine;
In
diethyl ether;
|
|
|
With
bromine;
In
diethyl ether;
at 10 ℃;
|
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
at 20 ℃;
for 2h;
|
86 % Chromat.
|
|
With
N-Bromosuccinimide;
In
diethyl ether;
at 30 ℃;
for 2h;
UV-irradiation;
|
|
|
|
|
|
With
bromine;
In
ethyl acetate;
|
|
|
With
sodium hypochlorite; bromine;
In
acetic acid;
|
|
|
With
1,1'-(ethane-1,2-diyl)dipyridinium bistribromide;
In
acetonitrile;
for 0.166667h;
|
|
|
With
N-Bromosuccinimide; amberlyst-15(R);
In
ethyl acetate;
at 20 ℃;
for 24h;
|
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
In
dichloromethane;
at 0 - 20 ℃;
|
|
|
With
N-Bromosuccinimide; acetic acid;
at 20 ℃;
Reflux;
|
|
|
With
aluminum (III) chloride; bromine;
In
diethyl ether;
at 0 - 20 ℃;
Inert atmosphere;
|
|
|
With
bromine;
In
tetrahydrofuran; diethyl ether;
at 20 ℃;
for 2h;
Inert atmosphere;
Cooling with ice;
|
|
|
Multi-step reaction
with
2
steps
1: triphenyl phosphite; bromine; triethylamine / dichloromethane / 20 h / -78 - 20 °C / Inert atmosphere
2: toluene-4-sulfonic acid; [hydroxy(tosyloxy)iodo]benzene / acetonitrile / 0.03 h / 20 °C / Inert atmosphere
With
triphenyl phosphite; [hydroxy(tosyloxy)iodo]benzene; bromine; toluene-4-sulfonic acid; triethylamine;
In
dichloromethane; acetonitrile;
|
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
In
dichloromethane;
at 0 ℃;
for 4h;
Inert atmosphere;
Reflux;
|
|
|
With
N-Bromosuccinimide; ammonium acetate;
In
diethyl ether;
at 0 - 20 ℃;
for 2h;
|
|
|
With
bromine;
In
methanol;
at 8 ℃;
Temperature;
|
|
|
With
tetrabutylammomium bromide; dihydrogen peroxide; trifluoroacetic acid;
In
water;
at 25 ℃;
for 24h;
Inert atmosphere;
|
76 %Spectr.
|
|
|
|
|
With
bromine;
In
diethyl ether;
at 0 - 20 ℃;
|
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
In
dichloromethane;
at 40 ℃;
for 1h;
Reflux;
|
|
|
With
hydrogen bromide; dimethyl sulfoxide;
In
ethyl acetate;
at 60 ℃;
for 6h;
|
|
|
With
N-Bromosuccinimide; toluene-4-sulfonic acid;
In
dichloromethane;
for 4h;
Reflux;
|
|
|
With
bromine;
In
chloroform;
at 0 - 20 ℃;
for 3h;
|
|
|
With
copper(ll) bromide;
In
ethyl acetate;
at 20 ℃;
|
2.What is the CAS number for 2-Bromo-1-tetralone ?
The CAS number of 2-Bromo-1-tetralone is 13672-07-6.
More information of 2-Bromo-1-tetralone 13672-07-6 are:
|
CAS?Number |
13672-07-6 |
|
Density |
1.529g/cm3 |
|
Melting Point |
39-43 ºC |
|
Boiling Point |
64-67 ºC (0.06 mmHg) |
|
Flash Point |
98.4°C |
|
Vapor Pressure |
0.000857mmHg at 25°C |
|
Refractive Index |
1.609 |
|
PSA |
17.07000 |
|
LogP |
2.57900 |
3.What are another words for 2-Bromo-1-tetralone ?
Synonyms?for?2-Bromo-1-tetralone 13672-07-6:2-Bromo-1-oxotetralin;2-Bromo-1-tetralone; 2-Bromo-3,4-dihydro-1(2H)-naphthalenone;2-Bromo-3,4-dihydro-2H-naphthalen-1-one; 2-Bromo-a-tetralone; 2-Bromotetralone;3,4-Dihydro-2-bromo-1(2H)-naphthalenone; NSC 402212
4.What is the molecular formula of 2-Bromo-1-tetralone?
The chemical formula of ?2-Bromo-1-tetralone is?C10 H9 BrO which containing 10 Carbon atoms,9 Hydrogen atoms,1 Bromine atoms and 1 Oxygen atoms,and the molecular weight of??2-Bromo-1-tetralone?is 225.085.
5.What is 2-Bromo-1-tetralone (13672-07-6) used for?
2-Bromo-1-tetralone is an organic compound classified as a bromoarene. It is a white to off-white solid that serves as a versatile intermediate in the synthesis of various pharmaceuticals and organic compounds. Known for its role in the production of biologically active molecules, 2-Bromo-1-tetralone is a valuable building block in both laboratory research and commercial production.
InChI:InChI=1/C10H9BrO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-4,9H,5-6H2
Relevant articles related to 2-Bromo-1-tetralone:
|
Article |
Source |
|
One-pot synthesis of 4-alkoxybenzo[c]thiophenes |
Akbarzadeh, Tahmineh,Shafiee, Abbas , p. 1455 - 1462 (2004) |
|
A Method for the Catalytic Enantioselective Synthesis of Chiral α-Azido and α-Amino Ketones from Racemic α-Bromo Ketones, and Its Generalization to the Formation of Bonds to C, O, and S |
Da Silva Gomes, Roberto,Corey , p. 20058 - 20061 (2019) |
6.Buy 2-Bromo-1-tetralone with the best price .
Chuanggao New Bio-Technical Material Co., Ltd is a quality supplier of 2-Bromo-1-tetralone. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on 2-Bromo-1-tetralone 13672-07-6.
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