3153-36-4
- Product Name：Ethyl 4-chlorobutyrate
- Molecular Formula：C6H11ClO2
- Purity：98% GC
- Molecular Weight：150.605
Product Details
Top quality factory supply 3153-36-4 Ethyl 4-chlorobutyrate at low price
- Molecular Formula:C6H11ClO2
- Molecular Weight:150.605
- Appearance/Colour:clear yellow to brownish liquid
- Vapor Pressure:0.678mmHg at 25°C
- Melting Point:-70oC
- Refractive Index:n20/D 1.432(lit.)
- Boiling Point:186 °C at 760 mmHg
- Flash Point:51.7 °C
- PSA：26.30000
- Density:1.057 g/cm3
- LogP:1.56850
ETHYL 4-CHLOROBUTYRATE(Cas 3153-36-4) Usage
|
Synthesis Reference(s) |
Synthesis, p. 538, 1973 DOI: 10.1055/s-1973-22254 |
InChI:InChI=1/C6H11ClO2/c1-2-9-6(8)4-3-5-7/h2-5H2,1H3
3153-36-4 Relevant articles
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Noyce,Canfield
, p. 3630 (1954)
-
A General Approach to Deboronative Radical Chain Reactions with Pinacol Alkylboronic Esters
André-Joyaux, Emy,Kuzovlev, Andrey,Renaud, Philippe,Tappin, Nicholas D. C.
supporting information, p. 13859 - 13864 (2020/06/10)
The generation of carbon-centered radica...
Synthesis and biological evaluation of new quinoxaline derivatives of ICF01012 as melanoma-targeting probes
El Aissi, Radhia,Liu, Jianrong,Besse, Sophie,Canitrot, Damien,Chavignon, Olivier,Chezal, Jean-Michel,Miot-Noirault, Elisabeth,Moreau, Emmanuel
supporting information, p. 468 - 473 (2014/06/09)
The aim of this study was the synthesis ...
PYRAZOLYL DERIVATIVES AS SYK INHIBITORS
-
Page/Page column 134, (2014/01/09)
The present invention provides novel pyr...
Easy and selective method for the synthesis of various mono-O- functionalized Calix[4]arenes: De-O-functionalization using TiCl4
Bois, Joackim,Espinas, Jeff,Darbost, Ulrich,Felix, Caroline,Duchamp, Christian,Bouchu, Denis,Taoufik, Mostafa,Bonnamour, Isabelle
experimental part, p. 7550 - 7558 (2011/02/25)
An efficient and selective method for th...
3153-36-4 Process route
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-
ethyl 4-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butanoate
-
-
3153-36-4
4-chloro-butyric acid ethyl ester
| Conditions | Yield |
|---|---|
|
With
trimethylsilyl trifluoromethanesulfonate; 4-tert-Butylcatechol; 2-methoxybenzo[d][1,3,2]dioxaborole; trans-di-O-tert-butyl hyponitrite;
In
methanol; dichloromethane; benzene;
at 70 ℃;
for 16h;
Inert atmosphere;
|
30% |
-
-
627-00-9
γ-chlorobutyric acid
-
-
64-17-5
ethanol
-
-
3153-36-4
4-chloro-butyric acid ethyl ester
| Conditions | Yield |
|---|---|
|
With
sulfuric acid;
|
|
|
With
thionyl chloride;
at 0 ℃;
for 2h;
Reflux;
|
|
|
With
acetyl chloride;
at 20 ℃;
for 24h;
Inert atmosphere;
|
3153-36-4 Upstream products
-
123-91-1
1,4-dioxane
-
14077-66-8
4-ethoxy-butyryl chloride
-
96-48-0
4-butanolide
-
64-17-5
ethanol
3153-36-4 Downstream products
-
627-00-9
γ-chlorobutyric acid
-
4606-07-9
ethyl cyclopropylcarboxylate
-
63449-37-6
ethyl 4-<(2-ethoxy-2-oxoethyl)sulfanyl>butanoate
-
101583-01-1
2-cyano-2-phenyldiethyl adipate
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