ChemicalBook > CAS DataBase List > 5-chloro-3-hydroxyisothiazole

5-chloro-3-hydroxyisothiazole

Product Name
5-chloro-3-hydroxyisothiazole
CAS No.
25629-58-7
Chemical Name
5-chloro-3-hydroxyisothiazole
Synonyms
hydroxyisothiazole;5-chloroisothiazol-3-ol;5-Chloro-3-isothiazolol;5-chloroisothiazol-3-one;5-Chloroisothiazol-3(2H)-one;5-Chloro-3(2H)-isothiazolone;5-chloro-3-hydroxyisothiazole;5-Chloro-4-isothiazolin-3-one;3(2H)-Isothiazolone, 5-chloro-;5-chloro-3(2H)-Isothiazolone 97%
CBNumber
CB92549513
Molecular Formula
C3H2ClNOS
Formula Weight
135.57
MOL File
25629-58-7.mol
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5-chloro-3-hydroxyisothiazole Property

Melting point:
96-97 °C(Solv: water (7732-18-5))
Density 
1.62±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
7.20±0.40(Predicted)
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Safety

HS Code 
2934100090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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N-Bromosuccinimide Price

TRC
Product number
B423970
Product name
5-chloroisothiazol-3-ol
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
B423970
Product name
5-chloroisothiazol-3-ol
Packaging
100mg
Price
$240
Updated
2021/12/16
Matrix Scientific
Product number
094246
Product name
5-Chloroisothiazol-3-ol
Purity
95+%
Packaging
250mg
Price
$385
Updated
2021/12/16
AK Scientific
Product number
Z4502
Product name
5-Chloroisothiazol-3-ol
Packaging
1g
Price
$440
Updated
2021/12/16
AK Scientific
Product number
Z4502
Product name
5-Chloroisothiazol-3-ol
Packaging
100mg
Price
$143
Updated
2021/12/16
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5-chloro-3-hydroxyisothiazole Chemical Properties,Usage,Production

Synthesis

5-chloro-3-hydroxyisothiazole can be synthesized from 3,3'-disulfanediyldipropionic acid and Thionyl chloride in three steps. In particular, in the last step, 5-chloro isothiazolone derivatives (5-chloro-3-hydroxyisothiazole) were the predominant products when the ratio of sulfuryl chloride/amide was 3:1 while with the relevant ratio of 1:1, the 5-unsubstituted analogs were the predominant products[1].

References

[1] Khalaj A, et al. Synthesis and antibacterial activity of 2-(4-substituted phenyl)-3(2H)-isothiazolones. European Journal of Medicinal Chemistry, 2004; 39: 285–290.

5-chloro-3-hydroxyisothiazole Preparation Products And Raw materials

Raw materials

Preparation Products

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