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(S)-2-amino-3-hydroxypropionamide
  • Chemical Name: (S)-2-amino-3-hydroxypropionamide
  • CAS No.: 6791-49-7

Bulk supply high purity (S)-2-amino-3-hydroxypropionamide 6791-49-7, Paid sample available

  • Molecular Formula: C3H8 N2 O2
  • Molecular Weight: 104.109
  • Vapor Pressure: 8.9E-10mmHg at 25°C 
  • Boiling Point: 444.7°C at 760 mmHg 
  • Flash Point: 222.8°C 
  • PSA: 89.34000 
  • Density: 1.294g/cm3 
  • LogP: -0.80810 

(S)-2-amino-3-hydroxypropionamide(Cas 6791-49-7) Usage

General Description

(S)-2-amino-3-hydroxypropionamide, also known as (S)-serine, is a naturally occurring compound and a non-essential amino acid. It plays a crucial role in the biosynthesis of proteins and is also involved in the metabolism of purines and pyrimidines. This chemical is a key component of many important biological processes, including the synthesis of phospholipids, nucleotides, and the neurotransmitter glycine. It is also involved in the formation of the antioxidant glutathione and is important for the maintenance of muscle and immune function. (S)-2-amino-3-hydroxypropionamide is typically obtained through the diet, as it is found in various food sources such as meat, dairy, and soy products, and it can also be synthesized in the body from other amino acids.

InChI:InChI=1/C3H8N2O2/c4-2(1-6)3(5)7/h2,6H,1,4H2,(H2,5,7)

6791-49-7 Relevant articles

HEMIAMINAL-TAG FOR PROTEIN LABELING AND PURIFICATION

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Page/Page column 22; 24, (2018/06/30)

The invention pertains to the synthesis,...

Synthetic method for chiral alpha-aminoamide compounds

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Paragraph 0056; 0057; 0058, (2018/01/11)

The invention provides a synthetic metho...

Derivative of hyaluronic acid modified with amino-carboxylic acid

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, (2016/02/12)

The present invention provides a hyaluro...

BIARYL HETEROCYCLIC AMINES, AMIDES, AND SULFUR-CONTAINING COMPOUNDS AND METHODS OF MAKING AND USING THE SAME

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Page/Page column 64; 65, (2008/06/13)

The present invention relates generally ...

6791-49-7 Process route

methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride
5680-80-8

methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride

L-serinamide
6791-49-7

L-serinamide

Conditions
Conditions Yield
With ammonium hydroxide; at 20 ℃; for 5h;
96%
(S)-N-(tert-butoxycarbonyl)serine
3262-72-4

(S)-N-(tert-butoxycarbonyl)serine

L-serinamide
6791-49-7

L-serinamide

Conditions
Conditions Yield
(S)-N-(tert-butoxycarbonyl)serine; With pyridine; di-tert-butyl dicarbonate; ammonium bicarbonate; In 1,4-dioxane; at 20 ℃; for 16h;
With trifluoroacetic acid; at 20 ℃; for 0.5h;

6791-49-7 Upstream products

  • 70897-15-3
    70897-15-3

    N-α-carbobenzoxy-L-serinamide

  • 2788-84-3
    2788-84-3

    (S)-serine methyl ester

  • 3262-72-4
    3262-72-4

    (S)-N-(tert-butoxycarbonyl)serine

  • 5680-80-8
    5680-80-8

    methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride

6791-49-7 Downstream products

  • 56-45-1
    56-45-1

    L-serin

  • 129678-29-1
    129678-29-1

    Bz-Tyr-Ser-NH2