ChemicalBook > CAS DataBase List > N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE

N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE

Product Name
N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE
CAS No.
81112-08-5
Chemical Name
N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE
Synonyms
N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE;Acetamide, N-[4-(2-chloro-1-oxopropyl)phenyl]-
CBNumber
CB6298528
Molecular Formula
C11H12ClNO2
Formula Weight
225.67
MOL File
Mol file
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N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE Property

Melting point:
119-120 °C(Solv: ethanol (64-17-5); water (7732-18-5))
Boiling point:
429.9±25.0 °C(Predicted)
Density 
1.237±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
14.47±0.70(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C350925
Product name
N-[4-(2-Chloropropanoyl)phenyl]acetamide
Packaging
500mg
Price
$155
Updated
2021/12/16
AK Scientific
Product number
7210AJ
Product name
N-[4-(2-Chloropropanoyl)phenyl]acetamide
Packaging
1g
Price
$76
Updated
2021/12/16
AK Scientific
Product number
7210AJ
Product name
N-[4-(2-Chloropropanoyl)phenyl]acetamide
Packaging
5g
Price
$114
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0062010
Product name
N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE
Purity
95.00%
Packaging
1G
Price
$794.34
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0062010
Product name
N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE
Purity
95.00%
Packaging
2.5G
Price
$1119.71
Updated
2021/12/16
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N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE Chemical Properties,Usage,Production

Synthesis

7623-09-8

103-84-4

81112-08-5

a) Synthesis of 1-(4-acetamidophenyl)-2-chloropropanone: 118 g (0.93 mol) of 2-chloropropionyl chloride was added slowly and dropwise over a period of 1.5 h to a mixture containing 69.2 g (0.50 mol) of N-phenylacetamide and 525 mL of carbon disulfide. Subsequently, 205 g (1.50 mol) of aluminum chloride was added to the reaction system and the mixture was heated to reflux for 1 hour. Upon completion of the reaction, the supernatant was decanted and the residue was hydrolyzed with 1900 mL of ice water and 385 mL of 4N hydrochloric acid. The precipitate formed was separated by filtration and the precipitate was dissolved in benzene. The benzene solution was azeotropically distilled using a Dean-Stark apparatus to remove water. The hot solution was treated with activated carbon (CXA) and cooled to give 102.4 g (yield: 90.82%) of the target compound 1-(4-acetamidophenyl)-2-chloropropanone as a micron colored powder. Melting point (Kofler assay): 120°C.

References

[1] Organic Letters, 2017, vol. 19, # 10, p. 2548 - 2551
[2] Patent: US5128349, 1992, A
[3] Patent: US4677228, 1987, A
[4] Patent: WO2018/86703, 2018, A1. Location in patent: Page/Page column 200
[5] Tetrahedron Letters, 1981, vol. 22, # 43, p. 4305 - 4308

N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE Suppliers

Accela ChemBio Inc.
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+1(858) 699-3322
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United States
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Synthonix Inc
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United States Biological
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Combi-Blocks Inc.
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Ryan Scientific, Inc.
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Country
United States
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81112-08-5, N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDERelated Search:


  • N-[4-(2-CHLOROPROPANOYL)PHENYL]ACETAMIDE
  • Acetamide, N-[4-(2-chloro-1-oxopropyl)phenyl]-
  • 81112-08-5
  • 811112-08-5