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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
Molecular Weight:
263.24
MDL Number:
MFCD21648243
MOL File:
112434-18-1.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:40
Product description Number Pack Size Price
BENZYL-(2,4-DIFLUOROPHENYL)CARBAMATE 95.00% HCH0368557 5MG $502.55
Benzyl 2,4-difluorophenylcarbamate 97% 071203 5g $615
Benzyl(2,4-difluorophenyl)carbamate 2182AA 5g $1546
benzyl(2,4-difluorophenyl)carbamate 95+% CM128599 5g $1036
Benzyl(2,4-difluorophenyl)carbamate 97% CD12179772 5g $1097

benzyl 2,4-difluorophenylcarbaMate Properties

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)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

benzyl 2,4-difluorophenylcarbaMate price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation HCH0368557 BENZYL-(2,4-DIFLUOROPHENYL)CARBAMATE 95.00% 112434-18-1 5MG $502.55 2021-12-16 Buy
Matrix Scientific 071203 Benzyl 2,4-difluorophenylcarbamate 97% 112434-18-1 5g $615 2021-12-16 Buy
AK Scientific 2182AA Benzyl(2,4-difluorophenyl)carbamate 112434-18-1 5g $1546 2021-12-16 Buy
Chemenu CM128599 benzyl(2,4-difluorophenyl)carbamate 95+% 112434-18-1 5g $1036 2021-12-16 Buy
Crysdot CD12179772 Benzyl(2,4-difluorophenyl)carbamate 97% 112434-18-1 5g $1097 2021-12-16 Buy
Product number Packaging Price Buy
HCH0368557 5MG $502.55 Buy
071203 5g $615 Buy
2182AA 5g $1546 Buy
CM128599 5g $1036 Buy
CD12179772 5g $1097 Buy

benzyl 2,4-difluorophenylcarbaMate Chemical Properties,Uses,Production

Synthesis

2,4-Difluoroaniline

367-25-9

Benzyl chloroformate

501-53-1

benzyl 2,4-difluorophenylcarbaMate

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

benzyl 2,4-difluorophenylcarbaMate Suppliers

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