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4-BroMothiazole-5-carbaldehyde

Product Name
4-BroMothiazole-5-carbaldehyde
CAS No.
1244948-92-2
Chemical Name
4-BroMothiazole-5-carbaldehyde
Synonyms
4-Bromothiazole-5-carbald;4-BroMothiazole-5-carbaldehyde;4-bromothiazole-5-carboxaldehyde;5-Thiazolecarboxaldehyde, 4-bromo-
CBNumber
CB22651686
Molecular Formula
C4H2BrNOS
Formula Weight
192.03
MOL File
1244948-92-2.mol
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4-BroMothiazole-5-carbaldehyde Property

Boiling point:
279.1±20.0 °C(Predicted)
Density 
1.920±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.83±0.10(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

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

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
B416848
Product name
4-Bromothiazole-5-carbaldehyde
Packaging
500mg
Price
$45
Updated
2021/12/16
TRC
Product number
B416848
Product name
4-Bromothiazole-5-carbaldehyde
Packaging
1g
Price
$60
Updated
2021/12/16
TRC
Product number
B416848
Product name
4-Bromothiazole-5-carbaldehyde
Packaging
5g
Price
$75
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0365891
Product name
4-BROMOTHIAZOLE-5-CARBALDEHYDE
Purity
95.00%
Packaging
5MG
Price
$503.29
Updated
2021/12/16
AK Scientific
Product number
9032BB
Product name
4-Bromothiazole-5-carbaldehyde
Packaging
250mg
Price
$522
Updated
2021/12/16
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4-BroMothiazole-5-carbaldehyde Chemical Properties,Usage,Production

Synthesis

262444-15-5

1244948-92-2

The general procedure for the synthesis of 4-bromo-5-formylthiazole from 4-bromo-5-hydroxymethylthiazole was carried out as follows: at room temperature, (4-bromothiazol-5-yl)methanol (870 mg) was dissolved in dichloromethane (25 mL) to form a light yellow solution. Subsequently, Dess-Martin periodinane (DMP, 2.16 g) was added to this solution and the reaction mixture was transformed into a yellow suspension. The reaction mixture was stirred continuously for 18 hours under argon protection and at room temperature. After completion of the reaction, ethyl acetate and saturated aqueous sodium bicarbonate solution were added to the reaction mixture and stirred for 5 minutes. Next, water was added and the mixture was extracted three times with dichloromethane. All organic layers were combined, dried with anhydrous magnesium sulfate, filtered and the solvent was evaporated under vacuum. Purification by column chromatography (using a Biotage system, SNAP 50g column, solvent A: heptane; solvent B: ethyl acetate; gradient elution procedure: keep 10% B for 5 column volumes of elution, then step up from 10% B to 30% B in 2 column volumes, and finally keep 30% B for 3 column volumes of elution) gave 708 mg of a yellow solid product. The product was characterized by 1H-NMR (CDCl3): δ 10.0 (s, 1H); 9.04 (s, 1H).

References

[1] Patent: WO2013/114332, 2013, A1. Location in patent: Page/Page column 108
[2] Patent: US2014/371204, 2014, A1. Location in patent: Paragraph 0796

4-BroMothiazole-5-carbaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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4-BroMothiazole-5-carbaldehyde Suppliers

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1244948-92-2, 4-BroMothiazole-5-carbaldehydeRelated Search:


  • 4-BroMothiazole-5-carbaldehyde
  • 4-Bromothiazole-5-carbald
  • 4-bromothiazole-5-carboxaldehyde
  • 5-Thiazolecarboxaldehyde, 4-bromo-
  • 1244948-92-2