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2-CHLORO-6-HYDROXYBENZALDEHYDE

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Products Intro: Product Name:2-CHLORO-6-HYDROXYBENZALDEHYDE
CAS:18362-30-6
Purity:99% Package:1KG;0.00;USD|25KG;0.00;USD
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Products Intro: Product Name:2-CHLORO-6-HYDROXYBENZALDEHYDE
CAS:18362-30-6
Purity:99%
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CAS:18362-30-6
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Products Intro: Product Name:2-Chloro-6-hydroxybenzaldehyde
CAS:18362-30-6
Purity:98%, 99% Package:100g, 500g, 1kg, 25kg
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Products Intro: Product Name:2-Chloro-6-hydroxybenzaldehyde
CAS:18362-30-6
Purity:98% (Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg

2-CHLORO-6-HYDROXYBENZALDEHYDE manufacturers

2-CHLORO-6-HYDROXYBENZALDEHYDE Basic information
Product Name:2-CHLORO-6-HYDROXYBENZALDEHYDE
Synonyms:2-chloro-6-hydroxy-benzaldehyd;6-CHLOROSALICYLALDEHYDE;2-CHLORO-6-HYDROXYBENZALDEHYDE;6-chloro salicyaldehyde;6-chloro salicyaldehyde 2-chloro-6-hydroxybenzaldehyde;Benzaldehyde, 2-chloro-6-hydroxy-;6-Chlorosalicylaldehyde, 3-Chloro-2-formylphenol;6-Chloro-2-hydroxybenzaldehyde
CAS:18362-30-6
MF:C7H5ClO2
MW:156.57
EINECS:
Product Categories:
Mol File:18362-30-6.mol
2-CHLORO-6-HYDROXYBENZALDEHYDE Structure
2-CHLORO-6-HYDROXYBENZALDEHYDE Chemical Properties
Melting point 51-55℃
Boiling point 223.1±20.0 °C(Predicted)
density 1.404±0.06 g/cm3(Predicted)
Fp 107℃
storage temp. 2-8°C
pka7.21±0.10(Predicted)
form powder to crystal
color White to Light yellow to Light orange
InChIInChI=1S/C7H5ClO2/c8-6-2-1-3-7(10)5(6)4-9/h1-4,10H
InChIKeyMVTWVXYIKIVAOJ-UHFFFAOYSA-N
SMILESC(=O)C1=C(O)C=CC=C1Cl
Safety Information
Hazard Codes Xn
Risk Statements 22-41
Safety Statements 26-39
WGK Germany 3
HS Code 2912490090
MSDS Information
2-CHLORO-6-HYDROXYBENZALDEHYDE Usage And Synthesis
Synthesis
2-Chloro-6-fluorobenzaldehyde

387-45-1

2-CHLORO-6-HYDROXYBENZALDEHYDE

18362-30-6

The general procedure for the synthesis of 6-chlorosalicylaldehyde from 2-chloro-6-fluoro-benzaldehyde was as follows: potassium hydroxide (10 g) was slowly added to a stirred solution of 2-chloro-6-fluoro-benzaldehyde (14.0 g, 88.3 mmol) in dimethyl sulfoxide (20 mL) at 0 °C. Subsequently, the reaction mixture was gradually warmed to room temperature and stirred continuously for 18 hours. Upon completion of the reaction, the reaction mixture was diluted with 100 mL of water and the pH was adjusted with concentrated hydrochloric acid to 2. The precipitate was collected by filtration, washed twice successively with 100 mL of water, and then dried with anhydrous sodium sulfate to afford the crude product, which was used in the subsequent reaction without further purification. The final yield was 8.5 g in 62% yield. The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3) with δppm 6.65-7.02 (m, 2H), 7.39-7.47 (m, 1H), 10.41 (s, 1H), 11.95 (s, 1H).

References[1] European Journal of Organic Chemistry, 2018, vol. 2018, # 25, p. 3348 - 3351
[2] Patent: WO2012/87229, 2012, A1. Location in patent: Page/Page column 14
[3] Patent: US2008/171754, 2008, A1. Location in patent: Page/Page column 89
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1993, # 12, p. 1345 - 1358
[5] Zeitschrift fuer Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, Biochemie, Biophysik, Biologie, 1972, vol. 27, p. 663 - 674
Tag:2-CHLORO-6-HYDROXYBENZALDEHYDE(18362-30-6) Related Product Information
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