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N-Cbz-2-Amino-1,3-propanediol

CAS No.
71811-26-2
Chemical Name:
N-Cbz-2-Amino-1,3-propanediol
Synonyms
N-Cbz-Serinol;N-Cbz-2-amino-1,3-propyldiol;N-Cbz-2-Amino-1,3-propanediol;Carbamic acid, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, phenylmethyl ester
CBNumber:
CB52500848
Molecular Formula:
C11H15NO4
Molecular Weight:
225.24
MDL Number:
MFCD11656821
MOL File:
71811-26-2.mol
MSDS File:
SDS
Last updated:2026-07-28 20:33:29
Product description Number Pack Size Price
N-Cbz-2-Amino-1,3-propanediol 97% AS21600 1g $29
N-Cbz-2-Amino-1,3-propanediol 97% AS21600 5g $84
N-Cbz-2-Amino-1,3-propanediol 97% AS21600 25g $157
Benzyl (1,3-dihydroxypropan-2-yl)carbamate 97% A121899 250mg $10
Benzyl (1,3-dihydroxypropan-2-yl)carbamate 97% A121899 1g $12
More product size

N-Cbz-2-Amino-1,3-propanediol Properties

Melting point 110.3-112.2 °C
Boiling point 457.644±45.00 °C(Press: 760.00 Torr)(predicted)
Density 1.255±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
storage temp. Sealed in dry,Room Temperature
pka 11.388±0.46(predicted)
Appearance White to off-white Solid

N-Cbz-2-Amino-1,3-propanediol price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS21600 N-Cbz-2-Amino-1,3-propanediol 97% 71811-26-2 1g $29 2026-06-04 Buy
Activate Scientific AS21600 N-Cbz-2-Amino-1,3-propanediol 97% 71811-26-2 5g $84 2026-06-04 Buy
Activate Scientific AS21600 N-Cbz-2-Amino-1,3-propanediol 97% 71811-26-2 25g $157 2026-06-04 Buy
Ambeed A121899 Benzyl (1,3-dihydroxypropan-2-yl)carbamate 97% 71811-26-2 250mg $10 2026-06-05 Buy
Ambeed A121899 Benzyl (1,3-dihydroxypropan-2-yl)carbamate 97% 71811-26-2 1g $12 2026-06-05 Buy
Product number Packaging Price Buy
AS21600 1g $29 Buy
AS21600 5g $84 Buy
AS21600 25g $157 Buy
A121899 250mg $10 Buy
A121899 1g $12 Buy

N-Cbz-2-Amino-1,3-propanediol Chemical Properties,Uses,Production

Synthesis

Benzyl chloroformate

501-53-1

N-Cbz-2-Amino-1,3-propanediol

71811-26-2

General procedure for the synthesis of benzyl (1,3-dihydroxypropan-2-yl) carbamate from benzyl chloroformate: to a stirred slurry of 1.00 g (4.24 mmol) of N-benzyloxycarbonyl-1,3-dihydroxy-2-aminopropane and 0.65 mL (4.7 mmol) of triethylamine in 10 mL of THF at 0°C under argon gas protection over a 10-minute period 0.6 mL (4.2 mmol) of benzyl chloroformate (Aldrich) was slowly added dropwise. The reaction mixture was gradually warmed to room temperature and stirred continuously for 14 hours. After completion of the reaction, the mixture was diluted with ether and filtered. The filtrate was concentrated by evaporation and the residue was dissolved in 25 mL of methanol, 2 drops of dioxane solution with 4N HCl were added and the solution was heated to 40°C and maintained for 30 minutes. The solvent was subsequently evaporated and the residue was ground with a hexane/ether solvent mixture to give benzyl (1,3-dihydroxypropan-2-yl)carbamate as a white solid in 92% yield (880 mg) with a melting point of 104-106 °C. The mass spectrum (electrospray, positive ion mode) showed a m/z of 226.

References

[1] Patent: US5962440, 1999, A

N-Cbz-2-Amino-1,3-propanediol Preparation Products And Raw materials

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N-Cbz-2-Amino-1,3-propanediol Spectrum

N-Cbz-2-Amino-1,3-propanediol Carbamic acid, N-[2-hydroxy-1-(hydroxymethyl)ethyl]-, phenylmethyl ester N-Cbz-Serinol N-Cbz-2-amino-1,3-propyldiol 71811-26-2