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benzyl 2,4-difluorophenylcarbaMate

Product Name
benzyl 2,4-difluorophenylcarbaMate
CAS No.
112434-18-1
Chemical Name
benzyl 2,4-difluorophenylcarbaMate
Synonyms
benzyl 2,4-difluorophenylcarbaMate;(2,4-Difluorophenyl)carbamic acid benzyl ester;Carbamic acid, N-(2,4-difluorophenyl)-, phenylmethyl ester
CBNumber
CB22552745
Molecular Formula
C14H11F2NO2
Formula Weight
263.24
MOL File
112434-18-1.mol
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benzyl 2,4-difluorophenylcarbaMate Property

Boiling point:
312.1±42.0 °C(Predicted)
Density 
1.329±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
11.69±0.70(Predicted)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

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

American Custom Chemicals Corporation
Product number
HCH0368557
Product name
BENZYL-(2,4-DIFLUOROPHENYL)CARBAMATE
Purity
95.00%
Packaging
5MG
Price
$502.55
Updated
2021/12/16
Matrix Scientific
Product number
071203
Product name
Benzyl 2,4-difluorophenylcarbamate
Purity
97%
Packaging
5g
Price
$615
Updated
2021/12/16
AK Scientific
Product number
2182AA
Product name
Benzyl(2,4-difluorophenyl)carbamate
Packaging
5g
Price
$1546
Updated
2021/12/16
Chemenu
Product number
CM128599
Product name
benzyl(2,4-difluorophenyl)carbamate
Purity
95+%
Packaging
5g
Price
$1036
Updated
2021/12/16
Crysdot
Product number
CD12179772
Product name
Benzyl(2,4-difluorophenyl)carbamate
Purity
97%
Packaging
5g
Price
$1097
Updated
2021/12/16
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benzyl 2,4-difluorophenylcarbaMate Chemical Properties,Usage,Production

Synthesis

367-25-9

501-53-1

112434-18-1

To a 250 mL round bottom flask was added 2,4-difluoroaniline (11.4 g, 4.62 mL, 45.4 mmol), dichloromethane (DCM, 103 mL) and pyridine (7.40 mL, 91 mmol). The reaction mixture was stirred at room temperature and benzyl chloroformate (8.15 mL, 54.5 mmol) was slowly added dropwise through the addition funnel. After the dropwise addition, the reaction mixture was continued to be stirred at room temperature overnight. Upon completion of the reaction, the mixture was poured into water and extracted with DCM. The organic phases were combined, washed sequentially with water and saturated saline, and then dried over anhydrous sodium sulfate. After filtration to remove the desiccant, the filtrate was concentrated under reduced pressure to afford benzyl (2,4-difluorophenyl)-carbamate (11.1 g, 42.2 mmol, 93% yield) as a white solid, which could be used for subsequent reactions without further purification.LC-MS (ESI, positive ion mode) analysis: calculated value of C14H11F2NO2 [M+H]+: 263.1; Measured value: 263.1. measured value [M+Na]+: 286.1. 1H NMR (400 MHz, DMSO-d6) δ ppm: 9.43 (br s, 1H), 7.51-7.66 (m, 1H), 7.24-7.46 (m, 6H), 7.01-7.12 (m, 1H), 5.15 (s, 2H).

References

[1] Tetrahedron Letters, 2006, vol. 47, # 36, p. 6393 - 6396
[2] Canadian Journal of Chemistry, 2009, vol. 87, # 2, p. 393 - 396
[3] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 10, p. 2215 - 2234
[4] Tetrahedron Letters, 2008, vol. 49, # 16, p. 2607 - 2610
[5] Patent: US2008/167338, 2008, A1. Location in patent: Page/Page column 44-45

benzyl 2,4-difluorophenylcarbaMate Preparation Products And Raw materials

Raw materials

Preparation Products

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112434-18-1, benzyl 2,4-difluorophenylcarbaMateRelated Search:


  • benzyl 2,4-difluorophenylcarbaMate
  • (2,4-Difluorophenyl)carbamic acid benzyl ester
  • Carbamic acid, N-(2,4-difluorophenyl)-, phenylmethyl ester
  • 112434-18-1