ChemicalBook > CAS DataBase List > 2,4-Dibromothiazole-5-methanol

2,4-Dibromothiazole-5-methanol

Product Name
2,4-Dibromothiazole-5-methanol
CAS No.
170232-68-5
Chemical Name
2,4-Dibromothiazole-5-methanol
Synonyms
2,4-Dibromothiazole-5-methanol;5-Thiazolemethanol, 2,4-dibromo-;(dibroMo-1,3-thiazol-5-yl)Methanol;2,4-DIBROMO-5-(HYDROXYMETHYL)THIAZOLE;(2,4-dibromo-1,3-thiazol-5-yl)methanol
CBNumber
CB12129454
Molecular Formula
C4H3Br2NOS
Formula Weight
272.95
MOL File
170232-68-5.mol
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2,4-Dibromothiazole-5-methanol Property

Boiling point:
349.0±27.0 °C(Predicted)
Density 
2.306±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
12.50±0.10(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
D424770
Product name
2,4-Dibromothiazole-5-methanol
Packaging
100mg
Price
$85
Updated
2021/12/16
Ark Pharm
Product number
P000097731
Product name
2,4-Dibromothiazole-5-methanol
Purity
95+%
Packaging
100mg
Price
$24
Updated
2021/12/16
Ark Pharm
Product number
P000097731
Product name
2,4-Dibromothiazole-5-methanol
Purity
95+%
Packaging
250mg
Price
$32
Updated
2021/12/16
Ark Pharm
Product number
P000097731
Product name
2,4-Dibromothiazole-5-methanol
Purity
95+%
Packaging
1g
Price
$79
Updated
2021/12/16
AK Scientific
Product number
W3711
Product name
2,4-Dibromothiazole-5-methanol
Packaging
250mg
Price
$82
Updated
2021/12/16
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2,4-Dibromothiazole-5-methanol Chemical Properties,Usage,Production

Synthesis

139669-95-7

170232-68-5

General procedure for the synthesis of 2,4-dibromothiazole-5-carboxaldehyde from 2,4-dibromothiazole-5-methanol: 2,4-dibromothiazole-5-carboxaldehyde (2.0 g, 7.4 mmol) was dissolved in methanol (80 mL) and NaBH4 (419 mg, 11.0 mmol) was added. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the reaction was quenched with 10% NaOH solution, diluted with water and extracted with ethyl acetate (2 times). The organic phases were combined and concentrated under reduced pressure to remove the solvent. The resulting crude product was purified by silica gel column chromatography with hexane/ethyl acetate (3:1, v/v) as eluent to give 2,4-dibromothiazole-5-methanol (1.84 g, 91% yield). Mass spectrum (DCI/NH3) showed m/z 274 (M+). 1H NMR (500 MHz, CDCl3) δ 2.11 (s, 1H), 4.78 (s, 2H).

References

[1] Synthetic Communications, 1995, vol. 25, # 17, p. 2639 - 2645
[2] Patent: WO2005/111003, 2005, A1. Location in patent: Page/Page column 143
[3] Patent: US2003/153752, 2003, A1
[4] Patent: US2003/153752, 2003, A1
[5] Patent: WO2016/193551, 2016, A1. Location in patent: Page/Page column 32

2,4-Dibromothiazole-5-methanol Preparation Products And Raw materials

Raw materials

Preparation Products

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2,4-Dibromothiazole-5-methanol Suppliers

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