1-(chloromethyl)-2-vinylbenzene
- Name:1-(chloromethyl)-2-vinylbenzene
- CAS:22570-84-9
- Purity:99%
Details
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- Molecular Formula:C9H9 Cl
- Molecular Weight:152.623
- Vapor Pressure:0.144mmHg at 25°C
- Boiling Point:223.4°Cat760mmHg
- Flash Point:87°C
- PSA:0.00000
- Density:1.066g/cm3
- LogP:3.06840
1-(chloromethyl)-2-vinylbenzene(Cas 22570-84-9) Usage
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General Description |
1-(Chloromethyl)-2-vinylbenzene, also known as styrene chloromethyl, is an organic compound with the chemical formula C9H9Cl. It is a colorless to pale yellow liquid with a strong, sweet odor. This chemical is commonly used in the production of polymers and resins, particularly polystyrene. It is a versatile compound that is also used in the production of synthetic rubber, fiberglass, and various plastic products. In addition, it is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. However, it is important to handle this chemical with caution as exposure to high levels of styrene chloromethyl can be harmful to human health, causing skin and eye irritation, respiratory issues, and potentially more serious long-term effects. |
InChI:InChI=1/C9H9Cl/c1-2-8-5-3-4-6-9(8)7-10/h2-6H,1,7H2
22570-84-9 Relevant articles
Hoveyda–Grubbs catalysts with an N→Ru coordinate bond in a six-membered ring. Synthesis of stable, industrially scalable, highly efficient ruthenium metathesis catalysts and 2-vinylbenzylamine ligands as their precursors
Polyanskii, Kirill B.,Alekseeva, Kseniia A.,Raspertov, Pavel V.,Kumandin, Pavel A.,Nikitina, Eugeniya V.,Gurbanov, Atash V.,Zubkov, Fedor I.
supporting information, p. 769 - 779 (2019/04/17)
A novel and efficient approach to the sy...
C- ARYL GLYCOSID DERIVATIVES, PHARMACEUTICAL COMPOSITION, PREPARATION PROCESS AND USES THEREOF
-
, (2017/04/19)
This invention relates to a kind of C-ar...
Preparation of conformationally constrained α2 antagonists: The bicyclo[3.1.0]hexane approach
Bonnaud, Bernard,Funes, Philippe,Jubault, Nathalie,Vacher, Bernard
, p. 3360 - 3369 (2007/10/03)
The aim of the research was to discover ...
Determining the scope of the lanthanide mediated, sequential hydroamination/C-C cyclization reaction: Formation of tricyclic and tetracyclic aromatic nitrogen heterocycles
Molander, Gary A.,Pack, Shawn K.
, p. 10581 - 10591 (2007/10/03)
The scope of the lanthanide mediated, se...
22570-84-9 Process route
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764-28-3
(E)-3,3'-(diazene-1,2-diyl)bis(2-methylpropanenitrile)
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100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene
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22570-84-9
2-chloromethylstyrene
| Conditions | Yield |
|---|---|
|
|
80% |
-
-
22826-55-7
N,N-dimethylaminomethylstyrene
-
-
22570-84-9
2-chloromethylstyrene
| Conditions | Yield |
|---|---|
|
With
potassium carbonate; methyl chloroformate;
In
tetrahydrofuran;
at -78 - 20 ℃;
for 0.166667h;
Inert atmosphere;
|
95% |
|
With
potassium carbonate; methyl chloroformate;
In
tetrahydrofuran;
at -78 - 20 ℃;
|
22570-84-9 Upstream products
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78317-75-6
1-(2-chloroethyl)-2-chloromethylbenzene
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87619-44-1
o-ethylbenzylidene chloride
-
149296-21-9
1-Chloromethyl-2-(2-mesyloxyethyl)benzene
-
22826-55-7
N,N-dimethylaminomethylstyrene
22570-84-9 Downstream products
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105519-14-0
N-(o-vinylbenzyl)-N-<(trimethylsilyl)methyl>amine
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149296-20-8
2-(2-Vinyl-benzyl)-malonic acid dimethyl ester
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171550-83-7
1-iodomethyl-2-vinyl-benzene
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877076-12-5
diethyl 2-(2-vinylbenzyl)malonate
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