(S)-Methyl 2-aminobutanoate

Product Name: (S)-Methyl 2-aminobutanoate
CAS No.: 15399-22-1
Chemical Name: (S)-Methyl 2-aminobutanoate
Synonyms: H-Abu-OMe;H-ABU-OME HCL;Levetiracetam-10;Methyl (2S)Levetiracetam Impurity J;Levetiracetam Impurity 14;Levetiracetam impuritiesJ;Methyl (2S)-Aminobutanoate;Levetiracetam impurities513;(S)-Methyl 2-aminobutanoate
CBNumber: CB9850868
Molecular Formula: C5H11NO2
Formula Weight: 117.15
MOL File: 15399-22-1.mol

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(S)-Methyl 2-aminobutanoate Property

Boiling point:: 127.8±13.0 °C(Predicted)
Density: 0.987±0.06 g/cm3(Predicted)
storage temp.: under inert gas (nitrogen or Argon) at 2–8 °C
pka: 7.89±0.29(Predicted)

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Safety

HS Code: 2922498590

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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

TRC

Product number: M285735
Product name: Methyl(2S)-2-Aminobutanoate
Packaging: 5g
Price: $250
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA107933
Product name: H-Abu-OMe·HCl
Packaging: 1g
Price: $94
Updated: 2021/12/16

Activate Scientific

Product number: AS47651
Product name: (S)-Methyl 2-aminobutanoate
Purity: 97% ee
Packaging: 1g
Price: $158
Updated: 2021/12/16

Activate Scientific

Product number: AS47651
Product name: (S)-Methyl 2-aminobutanoate
Purity: 97% ee
Packaging: 5G
Price: $430
Updated: 2021/12/16

AK Scientific

Product number: B311
Product name: Methyl(2S)-2-Aminobutanoate
Packaging: 5g
Price: $474
Updated: 2021/12/16

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(S)-Methyl 2-aminobutanoate Chemical Properties,Usage,Production

Uses

Methyl (2S)?-?2-?Aminobutanoate is a general chemical reagent used in the synthesis of methylsulphonamide based small molecule legumain inhibitors.

Synthesis

67-56-1

1492-24-6

2483-62-7

Step 1: Preparation of methyl (2S)-2-aminobutyrate; (2S)-2-aminobutyric acid (21.56 g, 0.21 mol) was dissolved in 120 mL of methanol. The reaction mixture was cooled to 0°C in an ice-water bath and thionyl chloride (30.5 mL, 0.42 mol) was added slowly and dropwise with continuous stirring. After the dropwise addition, the reaction mixture was heated to reflux for 2 hours and subsequently cooled to room temperature. The solvent was removed by concentration under reduced pressure to afford methyl (2S)-2-aminobutyrate (31.87 g, 99.3% yield) as a white solid.

References

[1] Patent: EP2481739, 2012, A1. Location in patent: Page/Page column 78
[2] Patent: US2012/184543, 2012, A1. Location in patent: Page/Page column 79
[3] Patent: WO2009/23655, 2009, A1. Location in patent: Page/Page column 53
[4] Journal of the American Chemical Society, 1991, vol. 113, # 11, p. 4297 - 4303
[5] Justus Liebigs Annalen der Chemie, 1961, vol. 649, p. 183 - 202

(S)-Methyl 2-aminobutanoate Preparation Products And Raw materials

Raw materials

Preparation Products

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(S)-Methyl 2-aminobutanoate Suppliers

China 57 India 2 United Kingdom 1 United States 5 Global 65

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15399-22-1, (S)-Methyl 2-aminobutanoateRelated Search:

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(S)-Methyl 2-aminobutanoate

ethyl (S)-2-aminobutanoate hydrochlori

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15399-22-1