CAS 79069-50-4

N-T-boc-L-alaninal

Description:

N-T-boc-L-alaninal is a chemical compound characterized by its structure, which includes a tert-butyloxycarbonyl (Boc) protecting group attached to the amino group of L-alanine, along with an aldehyde functional group. This compound is typically used in organic synthesis, particularly in peptide chemistry, as the Boc group serves to protect the amine during various reactions. The presence of the aldehyde functional group allows for further reactivity, enabling the compound to participate in condensation reactions or serve as an intermediate in the synthesis of more complex molecules. N-T-boc-L-alaninal is generally a white to off-white solid and is soluble in organic solvents such as dichloromethane and methanol. Its stability can be influenced by factors such as pH and temperature, making it essential to handle it under appropriate conditions to maintain its integrity. As with many chemical substances, safety precautions should be observed when handling N-T-boc-L-alaninal, including the use of personal protective equipment to avoid exposure.

Formula: C₈H₁₅NO₃

InChI: InChI=1/C8H15NO3/c1-6(5-10)9-7(11)12-8(2,3)4/h5-6H,1-4H3,(H,9,11)/t6-/m0/s1

SMILES: C[C@@H](C=O)N=C(O)OC(C)(C)C

Synonyms:

• Boc-L-alaninal
• tert-butyl [(1S)-1-methyl-2-oxoethyl]carbamate

Boc-Ala-aldehyde

CAS: 79069-50-4

Boc-L-alaninal.

Formula: C₈H₁₅NO₃

Purity: > 98%

Color and Shape: White Powder

Molecular weight: 173.21

Ref: 01-4033832

Boc-L-alaninal

CAS: 79069-50-4

Formula: C₈H₁₅NO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 173.2096

Ref: IN-DA0034JY

Boc-L-alaninal

CAS: 79069-50-4

Formula: C₈H₁₅NO₃

Molecular weight: 173.21

Ref: 7W-GL9428

Boc-Ala-aldehyde

CAS: 79069-50-4

Boc-Ala-aldehyde

Purity: 98%

Color and Shape: Solid

Molecular weight: 173.21g/mol

Ref: 54-OR963550

Boc-L-alanine aldehyde

CAS: 79069-50-4

Boc-L-alanine aldehyde is an isostere that can be used as a replacement for the amino acid L-alanine. It has been shown to have clinical use in the treatment of various diseases, including cancer, although it is not labelled for use. Boc-L-alanine aldehyde is synthesized by oxidation of L-alanine and its stereoselective synthesis has been demonstrated by ion exchange chromatography. The biosynthesis of this molecule has also been modeled using molecular modelling techniques. Boc-L-alanine aldehyde was modelled using quantum chemical calculations and was found to be enantiopure. This molecule can be used as the building block for peptidomimetics, which are molecules that mimic peptides with biological activity. Catalysis of this molecule has also been studied extensively.

Formula: C₈H₁₅NO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 173.21 g/mol

Ref: 3D-FB49474

(S)-tert-Butyl (1-oxopropan-2-yl)carbamate

CAS: 79069-50-4

Formula: C₈H₁₅NO₃

Purity: 97.0%

Color and Shape: Solid

Molecular weight: 173.212

Ref: 10-F405544