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1-(4-Bromophenyl)-butanol
- Chemical Name: 1-(4-Bromophenyl)-butanol
- CAS: 22135-53-1
- Purity: 99%
Factory supply good quality 1-(4-Bromophenyl)-butanol 22135-53-1 with stock
- Molecular Formula: C10H13 Br O
- Molecular Weight: 229.117
- Vapor Pressure: 0.000386mmHg at 25°C
- Boiling Point: 304.4°Cat760mmHg
- PKA: 14.22±0.20(Predicted)
- Flash Point: 137.9°C
- PSA： 20.23000
- Density: 1.35g/cm3
- LogP: 3.28260
1-(4-Bromophenyl)-butanol(Cas 22135-53-1) Usage
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General Description |
1-(4-Bromophenyl)-butanol is a chemical compound with the molecular formula C10H13BrO. It is a white to off-white solid with a molecular weight of 227.11 g/mol. 1-(4-Bromophenyl)-butanol is classified as an alcohol and contains a phenyl group and a bromine atom. It is used in organic synthesis and as a pharmaceutical intermediate. It has potential applications in the field of medicine and biochemistry, where it can be used to study biological systems and develop new medications. Additionally, it may also be used in the manufacturing of various products such as perfumes, flavors, and fragrances. Overall, 1-(4-Bromophenyl)-butanol has various potential uses in the chemical and pharmaceutical industries. |
InChI:InChI=1/C10H13BrO/c1-2-3-10(12)8-4-6-9(11)7-5-8/h4-7,10,12H,2-3H2,1H3
22135-53-1 Relevant articles
Synthesis of Benzylic Alcohols by C-H Oxidation
Tanwar, Lalita,B?rgel, Jonas,Ritter, Tobias
, p. 17983 - 17988 (2019/11/14)
Selective methylene C-H oxidation for th...
Highly enantioselective dynamic kinetic resolution of alkyl aryl carbinols carrying a trimethylsilyl group with a highly active lipoprotein lipase preparation
Cho, Jeonghun,Lee, Jusuk,Park, Jaiwook,Kim, Mahn-Joo
, p. 840 - 845 (2015/08/18)
Abstract The kinetic and dynamic kinetic...
Tandem α-Alkylation/Asymmetric Transfer Hydrogenation of Acetophenones with Primary Alcohols
Kovalenko, Oleksandr O.,Lundberg, Helena,Hübner, Dennis,Adolfsson, Hans
supporting information, p. 6639 - 6642 (2016/02/19)
Tandem α-alkylation/asymmetric transfer ...
Syntheses with organoboranes. XIII. Synthesis of ω-(4-bromophenyl)alkanoic acids and their borylation
Zaidlewicz, Marek,Wolan, Andrzej
, p. 129 - 135 (2007/10/03)
ω-(4-Bromophenyl)alkanoic acids 2c-e wer...
22135-53-1 Process route
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-
927-77-5
n-propylmagnesium bromide
-
-
1122-91-4
4-bromo-benzaldehyde
-
-
22135-53-1
1-(4'-bromophenyl)-1-butanol
| Conditions | Yield |
|---|---|
|
In
diethyl ether;
at 20 ℃;
|
90%
|
|
In
diethyl ether;
|
86%
|
|
With
diethyl ether;
|
|
|
In
tetrahydrofuran; diethyl ether;
at 0 - 25 ℃;
Inert atmosphere;
|
|
|
In
tetrahydrofuran;
for 2h;
|
-
-
106-94-5
propyl bromide
-
-
1122-91-4
4-bromo-benzaldehyde
-
-
22135-53-1
1-(4'-bromophenyl)-1-butanol
| Conditions | Yield |
|---|---|
|
propyl bromide;
With
magnesium;
In
diethyl ether;
for 1h;
Inert atmosphere;
Reflux;
4-bromo-benzaldehyde;
In
diethyl ether;
at -78 - 20 ℃;
Inert atmosphere;
|
22135-53-1 Upstream products
-
123-72-8
butyraldehyde
-
18620-02-5
(4-bromophenyl)magnesium bromide
-
927-77-5
n-propylmagnesium bromide
-
1122-91-4
4-bromo-benzaldehyde
22135-53-1 Downstream products
-
490035-78-4
(E)-1-bromo-4-(but-1-en-1-yl)benzene
-
74532-94-8
1-bromo-4-(but-1-en-1-yl)benzene
-
35656-89-4
4-(4-bromophenyl)butanoic acid
-
98453-57-7
4-(4-bromophenyl)butanoic acid methyl ester
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