CAS 3850-40-6

Serine,N-[(1,1-dimethylethoxy)carbonyl]-

Description:

Serine, N-[(1,1-dimethylethoxy)carbonyl]-, also known by its CAS number 3850-40-6, is an amino acid derivative characterized by the presence of a serine backbone modified with a protective carbonyl group. This compound typically features a hydroxyl group (-OH) and an amino group (-NH2) characteristic of amino acids, along with an ethoxycarbonyl group that serves to protect the amino functionality during synthetic processes. The presence of the bulky 1,1-dimethylethoxy group enhances steric hindrance, which can influence the compound's reactivity and solubility. Serine itself is a polar amino acid, and the modifications can affect its interactions in biochemical pathways. This compound is often utilized in organic synthesis and peptide chemistry, particularly in the formation of peptide bonds and as a building block for more complex molecules. Its stability and reactivity make it valuable in various applications, including pharmaceuticals and biochemistry.

Formula: C₈H₁₅NO₅

Synonyms:

• DL-Serine,N-[(1,1-dimethylethoxy)carbonyl]-
• Serine, N-carboxy-, N-tert-butyl ester, DL-(8CI)
• Boc-DL-serine

Serine, N-[(1,1-dimethylethoxy)carbonyl]- (9CI)

CAS: 3850-40-6

Formula: C₈H₁₅NO₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 205.2084

Ref: IN-DA00C6Y1

2-((Tert-Butoxycarbonyl)Amino)-3-Hydroxypropanoic Acid

CAS: 3850-40-6

2-((Tert-Butoxycarbonyl)Amino)-3-Hydroxypropanoic Acid

Purity: 98%

Molecular weight: 205.21g/mol

Ref: 54-OR1009632

2-((tert-Butoxycarbonyl)amino)-3-hydroxypropanoic acid

CAS: 3850-40-6

Purity: 97%

Molecular weight: 205.2100067

Ref: 10-F869217

2-[(tert-butoxycarbonyl)amino]-3-hydroxypropanoic acid

CAS: 3850-40-6

2-[(tert-Butoxycarbonyl)amino]-3-hydroxypropanoic acid is a chiral, labile tertiary alcohol that has been synthesized from methyl 2-aminoethanol and sodium hydrogen carbonate. This compound acts as a precursor in the synthesis of threonine, which is used to produce amino acids that are essential for life. The reaction between 2-[(tert-butoxycarbonyl)amino]-3-hydroxypropanoic acid and sodium carbonate produces an alkene that reacts with reactive groups, such as hydroxyls or carbonyls. It also inhibits the formation of primary alcohols through its affinity for phenolic compounds.

Formula: C₈H₁₅NO₅

Purity: Min. 95%

Molecular weight: 205.21 g/mol

Ref: 3D-DAA85040