BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE
- Product Name
- BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE
- CAS No.
- 146553-06-2
- Chemical Name
- BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE
- Synonyms
- Duvelisib Impurity 1;Metaraminol Impurity 43;D-Alanine-N'-Methoxy-N'-Methylamide;BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE;N-Boc-D-alanine N'-Methoxy-N'-MethylaMide;(tert-butoxycarbonyl)-N-methoxy-N-methyl-D-alaninamide;(R)-tert-butyl 1-(Methoxy(Methyl)aMino)-1-oxopropan-2-ylcarbaMat;(R)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate;tert-butyl (R)-(1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate;(R)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate - [B91279]
- CBNumber
- CB02454665
- Molecular Formula
- C10H20N2O4
- Formula Weight
- 232.28
- MOL File
- 146553-06-2.mol
BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE Property
- Density
- 1.070±0.06 g/cm3(Predicted)
- storage temp.
- Store at Room Tem.
- pka
- 11.19±0.46(Predicted)
Safety
- HazardClass
- IRRITANT
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H320Causes eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- 057765
- Product name
- (R)-tert-Butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate
- Purity
- 95%
- Packaging
- 1g
- Price
- $53
- Updated
- 2021/12/16
- Product number
- 057765
- Product name
- (R)-tert-Butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate
- Purity
- 95%
- Packaging
- 5g
- Price
- $187
- Updated
- 2021/12/16
- Product number
- AAA0004942
- Product name
- D-ALANINE-N'-METHOXY-N'-METHYLAMIDE
- Purity
- 95.00%
- Packaging
- 5G
- Price
- $371.7
- Updated
- 2021/12/16
- Product number
- 057765
- Product name
- (R)-tert-Butyl 1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate
- Purity
- 95%
- Packaging
- 25g
- Price
- $667
- Updated
- 2021/12/16
- Product number
- 4464AD
- Product name
- (R)-tert-Butyl1-(methoxy(methyl)amino)-1-oxopropan-2-ylcarbamate
- Packaging
- 25g
- Price
- $950
- Updated
- 2021/12/16
BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE Chemical Properties,Usage,Production
Synthesis
15761-38-3
6638-79-5
146553-06-2
To an oven-dried 100 mL round-bottomed flask were added N-tert-butoxycarbonyl-L-alanine (3.0 g, 15.8 mmol), anhydrous CH2Cl2 (60 mL), and N,N-diisopropylethylamine (DIPEA, 2.5 mL, 14.2 mmol), and the resulting solution was cooled to 0 °C. 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC, 3.7 g, 19.0 mmol) and 1-hydroxybenzotriazole (HOBt, 2.6 g, 19.0 mmol) were added in batches over a period of 10 min at 0 °C. The mixture was stirred at 0 °C for 10 min, then N,O-dimethylhydroxylamine hydrochloride (1.9 g, 19.0 mmol) and DIPEA (3.3 mL, 19.0 mmol) were added. The mixture was continued to be stirred at 0 °C for 1 h, followed by warming up to 25 °C and kept for 16 h. The reaction was carried out at 0 °C. Upon completion of the reaction, the reaction mixture was diluted with CH2Cl2 (300 mL) and the organic layer was washed sequentially with 2N HCl (3 × 180 mL), saturated NaHCO3 solution (2 × 180 mL) and brine (2 × 180 mL). The organic phase was dried over anhydrous Na2SO4 and concentrated under reduced pressure to give a white solid amide product (3.6 g, 99% yield), which did not require further purification. Product characterization data: mp(CHCl3) 138-140 °C; 1H NMR (300 MHz, DMSO) δ 1.11 (d, J = 6.9 Hz, 3H), 1.33 (s, 9H), 3.07 (s, 3H), 3.69 (s, 3H), 4.36 (t, J = 6.9 Hz, 1H), 7.03 (d, J = 6.9 Hz, 1H); ESI MS: 4.36 (t, J = 6.9 Hz, 1H), 7.03 (d, J = 6.9 Hz, 1H). 1H); ESI MS: m/z 255 (M + Na)+. The above amide product (3.7 g, 15.8 mmol) was dissolved in anhydrous THF (100 mL) and cooled to 0°C. Lithium aluminum hydride (LiAlH4, 660 mg, 17.4 mmol) was added to this solution and the reaction was stirred for 20 min. After the completion of the reaction was monitored by TLC, the reaction was quenched with 5% HCl solution. The organic layer was evaporated and the aqueous phase was extracted with EtOAc (3 x 30 mL). The organic phases were combined, dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford tert-butyl (R)-1-(methoxy(methyl)amino)-1-oxo-2-propylcarbamate as a white solid (2.6 g, 94% yield), which did not require further purification. Product characterization data: mp(CHCl3) 82-84 °C; 1H NMR (300 MHz, DMSO) δ 1.09 (d, J = 7.5 Hz, 3H), 1.36 (s, 9H), 3.83 (t, J = 9.9 Hz, 1H), 7.33 (d, J = 5.7 Hz, 1H), 9.39 (s, 1H); ESI MS: m/z 173 (M + H)+, 196 (M + Na)+.
References
[1] Angewandte Chemie - International Edition, 2013, vol. 52, # 34, p. 8957 - 8960
[2] Angew. Chem., 2013, vol. 125, # 34, p. 9126 - 9129,4
[3] Journal of Labelled Compounds and Radiopharmaceuticals, 2014, vol. 57, # 4, p. 275 - 278
[4] Organic Letters, 2002, vol. 4, # 16, p. 2665 - 2668
[5] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 15, p. 3582 - 3586
BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE manufacturers
- Product
- BENZYL (2-OXO-2-PHENYLETHYL)CARBAMATE 146553-06-2
- Price
- US $0.00/kg
- Min. Order
- 1kg
- Purity
- 98%
- Supply Ability
- 1000kg
- Release date
- 2025-07-08