CAS 42989-85-5

tert-Boc-aminooxyacetic acid

Description:

Tert-Boc-aminooxyacetic acid, with the CAS number 42989-85-5, is a chemical compound characterized by the presence of an aminooxy functional group and a tert-butyloxycarbonyl (Boc) protecting group. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. The aminooxy group is known for its ability to form stable conjugates with carbonyl compounds, making it useful in various synthetic applications, particularly in the field of organic chemistry and bioconjugation. The Boc group serves as a protective group for amines, allowing for selective reactions without interfering with the aminooxy functionality. Tert-Boc-aminooxyacetic acid is often utilized in peptide synthesis and the development of drug delivery systems due to its reactivity and stability. Additionally, it may exhibit biological activity, which can be explored in medicinal chemistry. Proper handling and storage conditions are essential to maintain its integrity and reactivity, as with many chemical substances.

Formula: C₇H₁₃NO₅

InChI: InChI=1/C7H13NO5/c1-7(2,3)13-6(11)8-12-4-5(9)10/h4H2,1-3H3,(H,8,11)(H,9,10)

SMILES: CC(C)(C)OC(=NOCC(=O)O)O

Synonyms:

• Boc-(Nhoac)-Oh
• {[(Tert-Butoxycarbonyl)Amino]Oxy}Acetic Acid
• Bis-Boc-aminooxyacetic acid
• Boc-Aoa
• (Boc-Aminooxy)Acetic Acid

[(tert-Butoxycarbonyl)aminooxy]acetic Acid

CAS: 42989-85-5

Formula: C₇H₁₃NO₅

Purity: >98.0%(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 191.18

Ref: 3B-B3338

(Boc-aminooxy)acetic acid, 98+%

CAS: 42989-85-5

(Boc-aminooxy)acetic acid was employed to introduce a hydroxylamine moiety into peptides; reaction with an aldehyde to an oxime. It was used in the preparation of Boc-aminooxy tetra(ethylene glycol). This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfol

Formula: C₇H₁₃NO₅

Purity: 98+%

Molecular weight: 191.18

Ref: 02-H54109

Boc-AOAc-OH

CAS: 42989-85-5

Protected aminooxyacetic acid derivative for the incorporation of an N-terminal O-alkylhydroxylamine moiety, which is used in the chemoselective ligation of unprotected peptide fragments, for the conjugation to lipids and glycosides, and for the introduction of labels by oxime formation. Peptides containing AOAc may be cleaved selectively at the N-O bond with Zn/AcOH.

Formula: C₇H₁₃NO₅

Purity: > 98%

Color and Shape: White

Molecular weight: 191.18

Ref: 01-4038799

Boc-Aoa-OH

CAS: 42989-85-5

Formula: C₇H₁₃NO₅

Purity: 98%

Color and Shape: Solid

Molecular weight: 191.1818

Ref: IN-DA003BZN

Boc-Aoa

CAS: 42989-85-5

Boc-Aoa

Purity: 98%

Molecular weight: 191.18g/mol

Ref: 54-BIBP1015

t-Boc-aminooxyacetic Acid

Controlled Product

CAS: 42989-85-5

Applications A Boc-protected bifunctional linking reagent.
References Jimenez-Castells, C., et al.: Bioorg. Med. Chem. Lett., 17, 5155 (2007), Carmona, S., et al.: Mol. Pharm., 6, 706 (2009), Nagahori, N., et al.: Biochem., 48, 583 (2009),

Formula: C₇H₁₃NO₅

Color and Shape: Neat

Molecular weight: 191.18

Ref: TR-B200750

2-(((tert-Butoxycarbonyl)amino)oxy)acetic acid

CAS: 42989-85-5

Formula: C₇H₁₃NO₅

Purity: 98%

Color and Shape: White powder

Molecular weight: 191.183

Ref: 10-F236882