Cost-effective and customizable 4-N-PENTYLOXYBENZOYL CHLORIDE 36823-84-4 supplier
- Molecular Formula: C12H15ClO2
- Molecular Weight: 226.703
- Appearance/Colour: clear colorless to light yellow liquid
- Vapor Pressure: 0.000245mmHg at 25°C
- Melting Point: 160 ºC
- Refractive Index: 1.542-1.544
- Boiling Point: 324.5 °C at 760 mmHg
- Flash Point: 120.5 °C
- PSA： 26.30000
- Density: 1.101 g/cm3
- LogP: 3.63460
4-N-PENTYLOXYBENZOYL CHLORIDE(Cas 36823-84-4) Usage
InChI:InChI=1/C12H15ClO2/c1-2-3-4-9-15-11-7-5-10(6-8-11)12(13)14/h5-8H,2-4,9H2,1H3
36823-84-4 Relevant articles
Synthesis of new liquid-crystalline compounds from the 3-aryl-5- alkylpyrazole series
Kovganko,Kovganko
, p. 696 - 700 (2006)
A method was developed for the preparati...
Synthesis and characterization of novel rod-like ester-based liquid crystalline homologous series: Effect of tert-butyl tail on mesomorphism
Thakur, Shavi,Patel, Hemant N.
, p. 76 - 89 (2021/04/14)
A new rod-like homologous series consist...
Dependence of mesomorphism on terminal polar group in novel azoester series
Kher, Seema N.,Prajapati,Makwana,Chandra, Raviprakash S.
, p. 44 - 53 (2019/10/14)
Novel homologous series 4-(4′-n-alkoxy b...
Identification of Anti-Mycobacterial Biofilm Agents Based on the 2-Aminoimidazole Scaffold
Nguyen, T. Vu,Minrovic, Bradley M.,Melander, Roberta J.,Melander, Christian
, p. 927 - 937 (2019/03/26)
Tuberculosis (TB) remains a significant ...
Study of Y-shaped liquid crystalline materials with polar nitro substituent
Dixit, Sandhya
, p. 77 - 84 (2018/06/27)
A new homologous series of Y-shaped liqu...
36823-84-4 Process route
-
-
15872-41-0
4-(pentyloxy)benzoic acid
-
-
36823-84-4
4-pentyloxybenzoyl chloride
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
|
95%
|
|
With
thionyl chloride;
|
|
|
With
phosphorus pentachloride;
|
|
|
With
thionyl chloride;
In
benzene;
for 3h;
Heating;
|
|
|
With
thionyl chloride;
for 2h;
Heating;
|
|
|
With
thionyl chloride;
for 2h;
Heating;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride; N,N-dimethyl-formamide;
Heating;
|
|
|
With
pyridine; thionyl chloride;
In
toluene;
Heating;
|
|
|
With
thionyl chloride;
Heating;
|
|
|
With
thionyl chloride;
In
benzene;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
In
N,N-dimethyl-formamide;
for 1h;
Heating;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
Heating;
|
|
|
With
thionyl chloride;
Reflux;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
Reflux;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
In
toluene;
for 3h;
Reflux;
|
|
|
With
thionyl chloride;
for 3h;
Reflux;
|
|
|
With
thionyl chloride;
Reflux;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
Reflux;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
for 3h;
Reflux;
|
|
|
With
thionyl chloride;
|
|
|
With
thionyl chloride;
at 20 ℃;
Reflux;
|
|
|
With
thionyl chloride;
Heating;
|
|
|
With
hydrogenchloride; thionyl chloride;
In
water;
|
|
|
With
thionyl chloride;
In
benzene;
for 1h;
Reflux;
|
|
|
With
thionyl chloride;
for 3h;
Reflux;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 0 ℃;
for 1h;
Inert atmosphere;
|
|
|
With
thionyl chloride;
for 2h;
Reflux;
|
-
-
110-53-2
1-Bromopentane
-
-
36823-84-4
4-pentyloxybenzoyl chloride
| Conditions | Yield |
|---|---|
|
Multi-step reaction
with
2
steps
1: KOH / ethanol / Heating
2: SOCl2
With
potassium hydroxide; thionyl chloride;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: KOH / ethanol
2: SOCl2
With
potassium hydroxide; thionyl chloride;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: alcohol; KOH
2: SOCl2
With
potassium hydroxide; thionyl chloride; ethanol;
|
|
|
Multi-step reaction
with
2
steps
2: thionyl chloride / 2 h / Heating
With
thionyl chloride;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / Heating
2: thionyl chloride / 2 h / Heating
With
thionyl chloride;
In
ethanol;
|
|
|
Multi-step reaction
with
3
steps
1: sodium ethylate; ethanol
2: ethanolic KOH-solution
3: phosphorus (V)-chloride
With
potassium hydroxide; ethanol; phosphorus pentachloride; sodium ethanolate;
|
|
|
Multi-step reaction
with
2
steps
1: sodium methylate; methanol / Erwaermen des Reaktionsprodukts mit aethanol. Kalilauge
2: thionyl chloride
With
methanol; thionyl chloride; sodium methylate;
|
|
|
Multi-step reaction
with
2
steps
1.1: potassium hydroxide
1.2: Reflux
2.1: thionyl chloride / Reflux
With
thionyl chloride; potassium hydroxide;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / ethanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / ethanol / 4 h / Reflux
2: thionyl chloride / toluene / 3 h / Reflux
With
thionyl chloride; potassium hydroxide;
In
ethanol; toluene;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / Reflux
2: thionyl chloride / 3 h / Reflux
With
thionyl chloride; potassium hydroxide;
|
|
|
Multi-step reaction
with
2
steps
1: methanol / Reflux
2: thionyl chloride
With
thionyl chloride;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / ethanol
2: thionyl chloride / Heating
With
thionyl chloride; potassium hydroxide;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol / Reflux
2: thionyl chloride / Reflux
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol / Reflux
2: thionyl chloride / Reflux
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol / Reflux
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol / Reflux
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / ethanol
2: thionyl chloride
With
thionyl chloride; potassium hydroxide;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / ethanol; water / 24 h / Reflux
2: thionyl chloride / benzene / 1 h / Reflux
With
thionyl chloride; potassium hydroxide;
In
ethanol; water; benzene;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / ethanol
2: thionyl chloride / Heating
With
thionyl chloride; potassium hydroxide;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol / Reflux
2: thionyl chloride / 3 h / Reflux
With
thionyl chloride; potassium hydroxide;
In
methanol;
|
|
|
Multi-step reaction
with
2
steps
1: potassium hydroxide / methanol / Reflux
2: thionyl chloride / 2 h / Reflux
With
thionyl chloride; potassium hydroxide;
In
methanol;
1: |Williamson Ether Synthesis;
|
36823-84-4 Upstream products
-
15872-41-0
4-(pentyloxy)benzoic acid
-
110-53-2
1-Bromopentane
-
99-96-7
4-hydroxy-benzoic acid
-
120-47-8
Ethyl 4-hydroxybenzoate
36823-84-4 Downstream products
-
102708-57-6
4-pentyloxy-benzoic acid-(3-dimethylamino-1,2-dimethyl-propyl ester)
-
95979-80-9
1-(4-pentyloxy-benzoyl)-thiosemicarbazide
-
100618-14-2
4-pentyloxy-benzoic acid methylamide
-
27906-53-2
C31 H46 N2 O4
