104-97-2
- Product Name：Cyclopentylpropionyl chloride
- Molecular Formula：C8H13ClO
- Purity：99%
- Molecular Weight：160.644
Product Details;
CasNo： 104-97-2
Molecular Formula： C8H13ClO
Appearance： light yellow liquid
Chinese Manufacturer supply Cyclopentylpropionyl chloride 104-97-2 in stock with high standard
- Molecular Formula:C8H13ClO
- Molecular Weight:160.644
- Appearance/Colour:light yellow liquid
- Vapor Pressure:0.34mmHg at 25°C
- Refractive Index:n20/D 1.464(lit.)
- Boiling Point:199.499 °C at 760 mmHg
- Flash Point:84.444 °C
- PSA：17.07000
- Density:1.062 g/cm3
- LogP:2.72220
Cyclopentylpropionyl chloride(Cas 104-97-2) Usage
InChI:InChI=1/C8H13ClO/c9-8(10)6-5-7-3-1-2-4-7/h7H,1-6H2
104-97-2 Relevant articles
Synthesis and Evaluation of 1,3,4-Thiadiazole Derivatives Containing Cyclopentylpropionamide as Potential Antibacterial Agent
Zhang, Min,Xu, Weiming,Wei, Kun,Liu, Hongwu,Yang, Qin,Liu, Qin,Yang, Liyun,Luo, Yuqin,Xue, Wei
, (2019)
This study aimed to identify new strateg...
Remote Regioselective Radical C-H Functionalization of Unactivated C-H Bonds in Amides: The Synthesis of gem-Difluoroalkenes
Hu, Qu-Ping,Cheng, Jing,Wang, Ying,Shi, Jie,Wang, Bi-Qin,Hu, Ping,Zhao, Ke-Qing,Pan, Fei
, p. 4457 - 4462 (2021)
The site-selective functionalization of ...
Design and Synthesis of 2-Methyl-7-aminobenzoxazole as Auxiliary in the Palladium(II)-Catalyzed Arylation of a beta-Positioned C(sp3)-H Bond
Luo, Feihua,Yang, Jun,Li, Zhengkai,Xiang, Haifeng,Zhou, Xiangge
, p. 887 - 893 (2016)
A palladium(II)-catalyzed direct arylati...
Cationic lipid compound, composition containing same and application
-
Paragraph 0103, (2021/06/22)
The invention provides a cationic lipid ...
Remote Directed Isocyanation of Unactivated C(sp3)-H Bonds: Forging Seven-Membered Cyclic Ureas Enabled by Copper Catalysis
Zhang, Hongwei,Tian, Peiyuan,Ma, Lishuang,Zhou, Yulu,Jiang, Cuiyu,Lin, Xufeng,Xiao, Xiao
supporting information, p. 997 - 1002 (2020/02/15)
Reported herein is an unprecedented copp...
104-97-2 Process route
-
-
140-77-2
3-cyclopentylpropionic acid
-
-
104-97-2
cyclopentanepropanoyl chloride
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
In
toluene;
Heating;
|
100% |
|
With
thionyl chloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 23 ℃;
|
100% |
|
With
pyridine; thionyl chloride;
for 5h;
Reflux;
|
83.85% |
|
With
thionyl chloride;
|
|
|
With
oxalyl dichloride;
In
dichloromethane;
at 20 ℃;
for 2h;
|
|
|
With
oxalyl dichloride;
In
dichloromethane; N,N-dimethyl-formamide;
|
|
|
With
thionyl chloride;
In
tetrachloromethane;
at 25 - 65 ℃;
Product distribution / selectivity;
|
|
|
With
thionyl chloride;
at 65 - 70 ℃;
for 1.5h;
|
|
|
With
thionyl chloride;
In
tetrachloromethane;
at 65 ℃;
for 0.5h;
|
|
|
With
thionyl chloride;
In
N,N-dimethyl-formamide; toluene;
at 20 ℃;
Inert atmosphere;
|
|
|
With
oxalyl dichloride;
In
dichloromethane;
at 20 ℃;
|
|
|
With
oxalyl dichloride;
|
|
|
With
thionyl chloride; N,N-dimethyl-formamide;
In
toluene;
at 70 ℃;
for 3h;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 0 - 20 ℃;
for 2h;
|
|
|
With
oxalyl dichloride;
In
dichloromethane; N,N-dimethyl-formamide;
at 20 ℃;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 25 ℃;
|
|
|
With
oxalyl dichloride;
In
dichloromethane;
at 20 ℃;
Inert atmosphere;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 0 - 20 ℃;
Inert atmosphere;
Schlenk technique;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 0 - 20 ℃;
for 2h;
Inert atmosphere;
|
|
|
With
oxalyl dichloride; N,N-dimethyl-formamide;
In
dichloromethane;
at 20 ℃;
for 2h;
|
-
-
79-37-8
oxalyl dichloride
-
-
140-77-2
3-cyclopentylpropionic acid
-
-
104-97-2
cyclopentanepropanoyl chloride
| Conditions | Yield |
|---|---|
|
In
dichloromethane;
|
104-97-2 Upstream products
-
140-77-2
3-cyclopentylpropionic acid
-
79-37-8
oxalyl dichloride
104-97-2 Downstream products
-
508-99-6
hydrocortisone cypionate
-
509-00-2
21-(3-cyclopentyl-propionyloxy)-17-hydroxy-pregn-4-ene-3,11,20-trione
-
633-36-3
3,17β-bis-(3-cyclopentyl-propionyloxy)-estra-1,3,5(10)-triene
-
58-20-8
testosterone cypionate
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