Quality Factory Hot Selling 4-Chlorobenzyl mercaptan 6258-66-8 with Fast Shipping
- Molecular Formula: C7H7 Cl S
- Molecular Weight: 158.652
- Appearance/Colour: Clear, colorless liquid. With a stench.
- Melting Point: 19-20 °C(lit.)
- Refractive Index: n20/D 1.5893(lit.)
- Boiling Point: 125°C 35mm
- PKA: 9.32±0.10(Predicted)
- Flash Point: 76 ºC
- PSA： 38.80000
- Density: 1.2
- LogP: 2.76980
4-Chlorobenzyl mercaptan(Cas 6258-66-8) Usage
InChI:InChI=1/C7H7ClS/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2
6258-66-8 Relevant articles
Benzylic Thio and Seleno Newman-Kwart Rearrangements
Eriksen, Kristina,Ulfkj?r, Anne,S?lling, Theis I.,Pittelkow, Michael
, p. 10786 - 10797 (2018/09/06)
The thermally induced OBn → SBn and OBn ...
Nonenzymatic Dynamic Kinetic Resolution of in situ Generated Hemithioacetals: Access to 1,3-Disubstituted Phthalans
Nath, Utpal,Chowdhury, Deepan,Pan, Subhas Chandra
, p. 1628 - 1633 (2018/03/21)
The first nonenzymatic DKR reaction of h...
Novelties of selective triphasic synthesis of bis-(p-chlorobenzyl) sulfide using hydrogen sulfide and reusable phase transfer catalyst
Jha, Preeti,Mondal, Ujjal,Gogoi, Devipriya,Singh, Gaurav,Sen, Sujit
, p. 30 - 40 (2016/04/26)
The present investigation is based on th...
Thiobencarb degradation by TiO2 photocatalysis: Parameter and reaction pathway investigations
Lai, Hsiao-Fang,Chen, Chiing-Chang,Wu, Ren-Jang,Lu, Chung-Shin
experimental part, p. 87 - 97 (2012/07/28)
The present study deals with the photoca...
6258-66-8 Process route
-
-
104-83-6
1-Chloro-4-(chloromethyl)benzene
-
-
6258-66-8
(4-chlorophenyl)methanethiol
| Conditions | Yield |
|---|---|
|
With
hydrosulfide exchange resin;
In
acetonitrile;
at 25 ℃;
for 0.25h;
|
93%
|
|
With
tetraethylammonium iodide; 1-(2-hydroxyethyl)-4,6-diphenylpyridin-2-thione;
In
acetonitrile;
for 24h;
Ambient temperature;
|
72%
|
|
With
sodium hydrogensulfide;
|
|
|
With
potassium hydrosulfide;
|
|
|
Multi-step reaction
with
2
steps
1: ethanol / 3 h / Heating
2: 10 N aq. NaOH / 0.33 h / 70 °C
With
sodium hydroxide;
In
ethanol;
|
|
|
Multi-step reaction
with
2
steps
1: acetone
2: aq.-ethanolic NaOH
With
sodium hydroxide; acetone;
|
-
-
104-83-6
1-Chloro-4-(chloromethyl)benzene
-
![1,1’-[thiobis(methylene)]bis[4-chlorobenzene]](/upload/2026/5/18096f50257f43ac8fbbab7ff78fbfe1_593f21c7-cac0-40af-9fef-a310993cddb4.png)
-
23566-23-6
1,1’-[thiobis(methylene)]bis[4-chlorobenzene]
-
-
6258-66-8
(4-chlorophenyl)methanethiol
| Conditions | Yield |
|---|---|
|
With
N-Methyldiethanolamine; hydrogen sulfide;
In
toluene;
at 49.84 ℃;
Temperature;
|
6258-66-8 Upstream products
-
28249-27-6
4-chlorobenzyl dimethylcarbamodithioate
-
104-83-6
1-Chloro-4-(chloromethyl)benzene
-
17356-08-0
thiourea
-
64-17-5
ethanol
6258-66-8 Downstream products
-
60116-21-4
2-(4-chloro-benzylsulfanyl)-ethylamine
-
104095-34-3
(4-chloro-benzyl)-[2]thienylmethyl sulfide
-
108881-33-0
S-(4-chlorobenzyl)benzothioate
-
101574-12-3
1,3-bis-(4-chloro-benzylsulfanyl)-propane
