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(6-AMino-5-broMo-pyridin-3-yl)-Methanol

Product Name
(6-AMino-5-broMo-pyridin-3-yl)-Methanol
CAS No.
1027785-19-8
Chemical Name
(6-AMino-5-broMo-pyridin-3-yl)-Methanol
Synonyms
6-AMino-5-broMopyridine-3-Methanol;3-Pyridinemethanol, 6-amino-5-bromo-;(6-AMino-5-broMo-pyridin-3-yl)-Methanol
CBNumber
CB72629426
Molecular Formula
C6H7BrN2O
Formula Weight
203.04
MOL File
1027785-19-8.mol
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(6-AMino-5-broMo-pyridin-3-yl)-Methanol Property

Boiling point:
344.4±37.0 °C(Predicted)
Density 
1.766±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
13.22±0.10(Predicted)
Appearance
Light brown to brown Solid
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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

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
A602215
Product name
(6-Amino-5-bromopyridin-3-yl)methanol
Packaging
100mg
Price
$90
Updated
2021/12/16
AK Scientific
Product number
3706DT
Product name
(6-Amino-5-bromopyridin-3-yl)methanol
Packaging
250mg
Price
$174
Updated
2021/12/16
Matrix Scientific
Product number
126923
Product name
(6-Amino-5-bromopyridin-3-yl)methanol
Purity
>95%
Packaging
1g
Price
$576
Updated
2021/12/16
Matrix Scientific
Product number
126923
Product name
(6-Amino-5-bromopyridin-3-yl)methanol
Purity
>95%
Packaging
5g
Price
$1710
Updated
2021/12/16
Ambeed
Product number
A206780
Product name
(6-Amino-5-bromopyridin-3-yl)methanol
Purity
97%
Packaging
100mg
Price
$58
Updated
2021/12/16
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(6-AMino-5-broMo-pyridin-3-yl)-Methanol Chemical Properties,Usage,Production

Synthesis

850429-51-5

1027785-19-8

General procedure for the synthesis of (6-amino-5-bromopyridin-3-yl)methanol from ethyl 6-amino-5-bromonicotinate: A) Ethyl 6-amino-5-bromonicotinate (2.31 g, 10 mmol) was dissolved in tetrahydrofuran (20 mL) at room temperature and lithium aluminum hydride (LAH, 10 mL, 1 M solution in tetrahydrofuran) was added slowly and dropwise. The reaction mixture was stirred for 1 h. The reaction was quenched by careful addition of water (0.2 mL). The resulting precipitate was collected by filtration and washed with ethyl acetate. The filtrate was concentrated under reduced pressure to give (6-amino-5-bromopyridin-3-yl)methanol (2.0 g, 99% yield) as a white solid. The product was confirmed by LC/MS analysis showing (M + H)+ = 203, 205 (ratio 1:1).1H NMR (CD3OD, 300 MHz) data were as follows: δ 7.79 (s, 1H), 7.67 (s, 1H), 4.35 (br s, 2H).

References

[1] Patent: WO2008/60907, 2008, A2. Location in patent: Page/Page column 34-35

(6-AMino-5-broMo-pyridin-3-yl)-Methanol Preparation Products And Raw materials

Raw materials

Preparation Products

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(6-AMino-5-broMo-pyridin-3-yl)-Methanol Suppliers

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1027785-19-8, (6-AMino-5-broMo-pyridin-3-yl)-MethanolRelated Search:


  • 6-AMino-5-broMopyridine-3-Methanol
  • 3-Pyridinemethanol, 6-amino-5-bromo-
  • (6-AMino-5-broMo-pyridin-3-yl)-Methanol
  • 1027785-19-8