ChemicalBook > CAS DataBase List > N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE

N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE

Product Name
N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE
CAS No.
98541-64-1
Chemical Name
N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE
Synonyms
N-Boc-L<;-serine beta-L;Boc L-Serine β-Lactone;N-Boc L-Serine -Lactone;N-Boc L-Serine b-Lactone;N-Boc L-Serine β-Lactone;Boc-L-Serine-beta-Lactone;N-BOC-L-SERINE BETA-LACTONE;(S)-3-BOC-AMINO-2-OXOOXETANE;N-Boc-L-serine β-lactone, >=97%
CBNumber
CB1741953
Molecular Formula
C8H13NO4
Formula Weight
187.19
MOL File
98541-64-1.mol
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N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE Property

Melting point:
117-119 °C
Boiling point:
319.0±31.0 °C(Predicted)
Density 
1.18±0.1 g/cm3(Predicted)
refractive index 
-26 ° (C=1, CH3CN)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Acetonitrile (Slightly), Chloroform (Slightly), DMSO (Slightly), Methanol(Slightly)
pka
10.53±0.20(Predicted)
form 
Solid
color 
White to Off-White
Stability:
Unstable in Solution
InChI
InChI=1S/C8H13NO4/c1-8(2,3)13-7(11)9-5-4-12-6(5)10/h5H,4H2,1-3H3,(H,9,11)/t5-/m0/s1
InChIKey
HRJDEHQWXAPGBG-YFKPBYRVSA-N
SMILES
C(OC(C)(C)C)(=O)N[C@H]1COC1=O
CAS DataBase Reference
98541-64-1
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Safety

Safety Statements 
24/25
HS Code 
29322090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TCI Chemical
Product number
B1995
Product name
N-(tert-Butoxycarbonyl)-L-serine beta-Lactone
Purity
>98.0%(N)
Packaging
1g
Price
$443
Updated
2025/07/31
TCI Chemical
Product number
B1995
Product name
N-(tert-Butoxycarbonyl)-L-serine beta-Lactone
Purity
>98.0%(N)
Packaging
5g
Price
$1330
Updated
2025/07/31
Usbiological
Product number
B2526-85
Product name
N-Boc L-Serine b-Lactone
Packaging
500mg
Price
$425
Updated
2021/12/16
TRC
Product number
B667390
Product name
N-BocL-Serineβ-Lactone
Packaging
2.5g
Price
$945
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB31428
Product name
Boc-L-serine-b-lactone
Packaging
250mg
Price
$50
Updated
2021/12/16
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N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE Chemical Properties,Usage,Production

Chemical Properties

White powder

Uses

An important -lactone inhibitor

Synthesis

3262-72-4

98541-64-1

The general procedure for the synthesis of N-(tert-butoxycarbonyl)-L-serine-β-lactone (AA2-1) from Boc-L-serine was as follows: to a dry 250 mL three-necked flask (equipped with a mechanical stirrer) under nitrogen protection was added triphenylphosphine (4.5 g, 17.1 mmol, 1.1 equiv.) and 100 mL of anhydrous THF:CH3CN (1:9 ) solvent mixture. The mixture was stirred until completely dissolved and then cooled to -55 °C (bath temperature). Dimethyl azodicarboxylate (DMAD, 1.9 mL, 17.1 mmol, 1.1 eq.) was slowly added dropwise over 10 minutes. After dropwise addition, stirring was continued for 20 minutes. Subsequently, Boc-Ser-OH (3.18 g, 15.5 mmol, 1.0 eq.) dissolved in 50 mL of anhydrous THF:CH3CN (1:9) was added dropwise over 30 minutes. The reaction mixture was stirred at -55 °C for 1.5 h. After removing the cooling bath, the reaction solution was allowed to slowly warm up to room temperature. After reaching room temperature, the solvent was removed by concentration under reduced pressure. The resulting yellow oil was purified by fast column chromatography [elution gradient: hexane:EtOAc (80:20) to (60:40)] to give 2.10 g AA2-1 as a white solid in 72% yield. It is recommended that purification of the feedstock be completed on the day of the reaction to avoid decomposition. DCM can be added if necessary to help dissolve the crude product.TLC assay conditions (Hex/EtOAc, 60/40): rf = 0.55 (CMA).

References

[1] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 3, p. 1330 - 1340
[2] Journal of the American Chemical Society, 1985, vol. 107, # 24, p. 7105 - 7109
[3] Patent: US2010/93720, 2010, A1. Location in patent: Page/Page column 37
[4] Heterocycles, 2001, vol. 55, # 1, p. 1 - 4
[5] Journal of Medicinal Chemistry, 1996, vol. 39, # 22, p. 4430 - 4438

N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE Suppliers

HBCChem, Inc.
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View Lastest Price from N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE manufacturers

Career Henan Chemical Co
Product
N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONE 98541-64-1
Price
US $1.00/g
Min. Order
1g
Purity
99.0%
Supply Ability
100 kg
Release date
2020-01-10

98541-64-1, N-(TERT-BUTOXYCARBONYL)-L-SERINE BETA-LACTONERelated Search:


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  • (S)-ALPHA-TERT-BUTOXYCARBONYLAMINO-BETA-PROPIOLACTONE
  • (S)-3-(TERT-BUTOXYCARBONYLAMINO)-2-OXETANONE
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  • N-BOC-L-SERINE BETA-LACTONE
  • [(3S)-2-oxo-3-oxetanyl]-1,1-dimethylethyl Ester Carbamic Acid
  • N-Boc L-Serine b-Lactone
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  • N-Boc L-Serine -Lactone
  • N-Boc-L-serine β-lactone, >=97%
  • (S)-3-BOC-AMINO-2-OXOOXETANE
  • Boc-L-Serine-beta-Lactone
  • (S)-alpha-Boc-amino-beta-propiolactone N-Boc-L-serine beta-Lactone (S)-3-(tert-Butoxycarbonylamino)-2-oxetanone (S)-alpha-tert-Butoxycarbonylamino-beta-propiolactone
  • Butoxycarbonylserinebetalactone
  • N-(tert-Butoxycarbonyl)-L-serine beta-lactone 98541-64-1
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  • N-(tert-Butoxycarbonyl)-L-serine β-Lactone
  • (S)-α-Boc-amino-β-propiolactone
  • tert-butyl N-[(3S)-2-oxooxetan-3-yl]carbamate
  • (S)-N-(tert-Butoxycarbonyl)-3-amino-2-oxetanone
  • tert-Butyl (S)-(2-oxooxetan-3-yl)carbamate
  • Boc L-Serine β-Lactone
  • N-Boc-<SC>L<
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  • (S)-tert-Butyl (2-oxooxetan-3-yl)carbamate - [B2081]
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  • Oxetanes
  • Simple 4-Membered Ring Compounds
  • Amines (Chiral)
  • Chiral Building Blocks
  • Amino Acids & Derivatives
  • Inhibitors
  • Amines (Chiral)
  • Chiral Building Blocks
  • Oxetanes
  • Simple 4-Membered Ring Compounds
  • Synthetic Organic Chemistry