CAS 28782-78-7

N-[(1,1-Dimethylethoxy)carbonyl]-L-alanylglycine

Description:

N-[(1,1-Dimethylethoxy)carbonyl]-L-alanylglycine, with the CAS number 28782-78-7, is a synthetic compound that belongs to the class of amino acid derivatives. This substance features a protective group, specifically the 1,1-dimethylethoxycarbonyl (also known as a tert-butoxycarbonyl or Boc group), which is commonly used in peptide synthesis to protect the amino group of amino acids. The compound is characterized by its structural components, including the L-alanine and glycine residues, which contribute to its properties as a dipeptide. It is typically a white to off-white solid and is soluble in organic solvents. The presence of the Boc group enhances its stability and facilitates further chemical modifications. This compound is primarily utilized in the field of organic chemistry and biochemistry, particularly in peptide synthesis and drug development, where the protection of functional groups is crucial for the selective formation of peptide bonds. Its reactivity and stability make it a valuable intermediate in the synthesis of more complex molecules.

Formula: C₁₀H₁₈N₂O₅

InChI: InChI=1S/C10H18N2O5/c1-6(8(15)11-5-7(13)14)12-9(16)17-10(2,3)4/h6H,5H2,1-4H3,(H,11,15)(H,12,16)(H,13,14)/t6-/m0/s1

InChI key: InChIKey=PBGVVLQMNSPMKN-LURJTMIESA-N

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

Synonyms:

• 2-[(2S)-2-[[(tert-Butoxy)carbonyl]amino]propanamido]acetic acid
• Glycine, N-(N-carboxy-<span class="text-smallcaps">L</span>-alanyl)-, N-tert-butyl ester
• Glycine, N-[(1,1-dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-alanyl-
• Glycine, N-[N-[(1,1-dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-alanyl]-
• N-(N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl)glycine
• N-(tert-Butoxycarbonyl)-<span class="text-smallcaps">L</span>-alanylglycine
• N-(tert-butoxycarbonyl)-L-alanylglycine
• N-[(1,1-Dimethylethoxy)carbonyl]-<span class="text-smallcaps">L</span>-alanylglycine
• N-tert-Butoxycarbonylalanylglycine
• t-Butoxycarbonyl-<span class="text-smallcaps">L</span>-alanylglycine
• t-Butoxycarbonyl-L-alanylglycine
• N-[(1,1-Dimethylethoxy)carbonyl]-L-alanylglycine
• Glycine, N-(N-carboxy-L-alanyl)-, N-tert-butyl ester
• Glycine, N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]-

(S)-2-(2-((Tert-Butoxycarbonyl)Amino)Propanamido)Acetic Acid

CAS: 28782-78-7

(S)-2-(2-((Tert-Butoxycarbonyl)Amino)Propanamido)Acetic Acid

Formula: C₁₀H₁₈N₂O₅

Purity: 98%

Molecular weight: 246.26

Ref: 54-OR1029773

(S);-2-(2-((tert-Butoxycarbonyl);amino);propanamido);acetic acid

CAS: 28782-78-7

Formula: C₁₀H₁₈N₂O₅

Purity: 97%

Color and Shape: Solid

Molecular weight: 246.2603

Ref: IN-DA002WFU

BOC-Ala-Gly

CAS: 28782-78-7

Formula: C₁₀H₁₈N₂O₅

Purity: 95%

Color and Shape: Solid

Molecular weight: 246.263

Ref: 10-F223797

Boc-Ala-Gly-OH

CAS: 28782-78-7

(S)-2-(2-((tert-Butoxycarbonyl)amino)propanamido)acetic acid

Formula: C₁₀H₁₈N₂O₅

Purity: 95%

Molecular weight: 246.26

Ref: IN-DG117750

Boc-Ala-Gly-OH

CAS: 28782-78-7

Boc-Ala-Gly-OH is a synthetic chemotactic peptide. It was originally synthesized in the form of an N-terminal amide and conjugated to a variety of carrier proteins, including bovine serum albumin, ovalbumin, thyroglobulin, and keyhole limpet hemocyanin. Boc-Ala-Gly-OH has been shown to stimulate the growth of various cell types including platelets and erythrocytes, as well as to inhibit tumor growth.

Formula: C₁₀H₁₈N₂O₅

Purity: Min. 95%

Molecular weight: 246.26 g/mol

Ref: 3D-FB111232