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6-Bromo-1-methylindolin-2-one

Product Name
6-Bromo-1-methylindolin-2-one
CAS No.
897957-06-1
Chemical Name
6-Bromo-1-methylindolin-2-one
Synonyms
6-Bromo-1-methylindolin-2-one;6-bromo-1-methyl-3H-indol-2-one;6-bromo-1-methyl-1,3-dihydro-indol-2-one;6-bromo-1-methyl-2,3-dihydro-1H-indol-2-one;6-bromo-1-methyl-1,3-dihydro-2H-indol-2-one;2H-Indol-2-one, 6-bromo-1,3-dihydro-1-methyl-
CBNumber
CB12727863
Molecular Formula
C9H8BrNO
Formula Weight
226.07
MOL File
897957-06-1.mol
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6-Bromo-1-methylindolin-2-one Property

Boiling point:
402.2±45.0 °C(Predicted)
Density 
1.589±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-0.82±0.20(Predicted)
Appearance
Off-white to pink Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H317May cause an allergic skin reaction

Precautionary statements

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

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N-Bromosuccinimide Price

TRC
Product number
B292875
Product name
6-Bromo-1-methylindolin-2-one
Packaging
5mg
Price
$60
Updated
2021/12/16
AK Scientific
Product number
8425DN
Product name
6-Bromo-1-methylindolin-2-one
Packaging
1g
Price
$258
Updated
2021/12/16
AK Scientific
Product number
8425DN
Product name
6-Bromo-1-methylindolin-2-one
Packaging
5g
Price
$822
Updated
2021/12/16
Chemenu
Product number
CM246116
Product name
6-Bromo-1-methylindolin-2-one
Purity
95%
Packaging
10g
Price
$877
Updated
2021/12/16
Crysdot
Product number
CD11024995
Product name
6-Bromo-1-methylindolin-2-one
Purity
97%
Packaging
10g
Price
$929
Updated
2021/12/16
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6-Bromo-1-methylindolin-2-one Chemical Properties,Usage,Production

Synthesis

667463-64-1

897957-06-1

General procedure for the synthesis of 6-bromo-1-methyldihydro-2-one from 6-bromo-1-methylindole-2,3-dione: 6-bromo-1-methyldihydro-2,3-dione (397 mg, 1.65 mmol) was mixed with hydrazine hydrate (1 mL, 20.6 mmol) and the reaction was heated to 100 °C for 1 h. The reaction was then warmed to 125 °C and continued for another hour. After completion of the reaction, the mixture was cooled to room temperature and layered with dichloromethane (DCM) and water. The aqueous layer was extracted twice with DCM and the organic layers were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure and the resulting residue was purified by column chromatography with the eluent cyclohexane/ethyl acetate (3:1, v/v). The product yield was 65%. Mass spectrometric analysis showed m/z 226 [M + H]+, m/z 224 [M + H]- with a retention time (rt) of 0.58 min (LC-MS method b).

References

[1] Patent: WO2013/41497, 2013, A1. Location in patent: Page/Page column 36
[2] Patent: WO2014/140075, 2014, A1. Location in patent: Page/Page column 215; 217
[3] Patent: WO2014/140081, 2014, A1. Location in patent: Page/Page column 61; 62
[4] Patent: US2014/275159, 2014, A1. Location in patent: Paragraph 0328; 0331
[5] Patent: WO2014/140091, 2014, A1. Location in patent: Page/Page column 74; 75

6-Bromo-1-methylindolin-2-one Preparation Products And Raw materials

Raw materials

Preparation Products

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6-Bromo-1-methylindolin-2-one Suppliers

A.J Chemicals
Tel
--
Fax
--
Email
sales@ajchem.in
Country
India
ProdList
6100
Advantage
58

897957-06-1, 6-Bromo-1-methylindolin-2-oneRelated Search:


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  • 6-bromo-1-methyl-2,3-dihydro-1H-indol-2-one
  • 6-Bromo-1-methylindolin-2-one
  • 2H-Indol-2-one, 6-bromo-1,3-dihydro-1-methyl-
  • 6-bromo-1-methyl-1,3-dihydro-2H-indol-2-one
  • 6-bromo-1-methyl-3H-indol-2-one
  • 897957-06-1