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(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE

Product Name
(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE
CAS No.
7048-38-6
Chemical Name
(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE
Synonyms
5-Chloro-2-methoxybenzeneacetonitrile;Benzeneacetonitrile, 5-chloro-2-methoxy-;2-(5-chloro-2-Methoxyphenyl)acetonitrile
CBNumber
CB01489169
Molecular Formula
C9H8ClNO
Formula Weight
181.62
MOL File
7048-38-6.mol
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(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE Property

Melting point:
63 °C(Solv: water (7732-18-5); ethanol (64-17-5))
Boiling point:
138-140 °C(Press: 1 Torr)
Density 
1.198±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Safety

HS Code 
2926907090
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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
C374538
Product name
(5-chloro-2-methoxyphenyl)acetonitrile
Packaging
100mg
Price
$65
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC139752
Product name
(5-Chloro-2-methoxyphenyl)acetonitrile
Packaging
500mg
Price
$70
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC139752
Product name
(5-Chloro-2-methoxyphenyl)acetonitrile
Packaging
1g
Price
$119
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC139752
Product name
(5-Chloro-2-methoxyphenyl)acetonitrile
Packaging
2g
Price
$207
Updated
2021/12/16
AK Scientific
Product number
0911AC
Product name
(5-Chloro-2-methoxyphenyl)acetonitrile
Packaging
1g
Price
$215
Updated
2021/12/16
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(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE Chemical Properties,Usage,Production

Synthesis

773837-37-9

7035-11-2

7048-38-6

The general procedure for the synthesis of 5-chloro-2-methoxyphenylacetonitrile from the compound (CAS: 773837-37-9) and 4-chloro-2-(chloromethyl)-1-methoxybenzene was as follows: compound Z-0-6 (32 g, 168 mmol) was dissolved in dimethyl sulfoxide (DMSO, 200 mL). Subsequently, sodium cyanide (29 g, 606 mmol) was added to the solution. The reaction mixture was heated to 80 °C under nitrogen protection and maintained at this temperature for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature, dispersed by the addition of water, and the product was subsequently separated by diafiltration. The filter cake was washed with a small amount of water and dried to give Z-0-7 (31 g, yield: 98.3%) as an orange-red solid.

References

[1] Patent: CN106243003, 2016, A. Location in patent: Paragraph 0130; 0131; 0136
[2] Patent: US2016/130239, 2016, A1. Location in patent: Paragraph 0735; 0739
[3] Patent: WO2014/151472, 2014, A1. Location in patent: Paragraph 00398-00399
[4] Patent: WO2016/40315, 2016, A1. Location in patent: Paragraph 00441; 00442
[5] Journal of Medicinal Chemistry, 2017, vol. 60, # 16, p. 7029 - 7042

(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE Preparation Products And Raw materials

Raw materials

Preparation Products

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(5-CHLORO-2-METHOXYPHENYL)ACETONITRILE Suppliers

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7048-38-6, (5-CHLORO-2-METHOXYPHENYL)ACETONITRILERelated Search:


  • 2-(5-chloro-2-Methoxyphenyl)acetonitrile
  • Benzeneacetonitrile, 5-chloro-2-methoxy-
  • 5-Chloro-2-methoxybenzeneacetonitrile
  • 7048-38-6