CAS 89711-08-0

tert-butyl N-(2-oxoethyl)carbamate

Description:

Tert-butyl N-(2-oxoethyl)carbamate is an organic compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonic acid derivative. This compound features a tert-butyl group, providing steric hindrance and influencing its reactivity and solubility. The presence of the 2-oxoethyl moiety suggests that it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Typically, compounds like this are utilized in organic synthesis, particularly in the formation of more complex molecules or as intermediates in pharmaceutical development. Its properties, such as solubility in organic solvents and stability under certain conditions, make it a valuable building block in synthetic chemistry. Additionally, the compound's structure may impart specific biological activities, making it of interest in medicinal chemistry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices.

Formula: C₇H₁₃NO₃

InChI: InChI=1/C7H13NO3/c1-7(2,3)11-6(10)8-4-5-9/h5H,4H2,1-3H3,(H,8,10)

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

Synonyms:

• Tert-Butyl (2-Oxoethyl)Carbamate
• N-Boc-2-aminoacetaldehyde
• Carbamic acid, N-(2-oxoethyl)-, 1,1-dimethylethyl ester

N-Boc-2-aminoacetaldehyde

CAS: 89711-08-0

Formula: HCOCH₂NHCO₂C(CH₃)₃

Molecular weight: 159.18

Ref: 7W-GL1557

N-Boc-2-aminoacetaldehyde

CAS: 89711-08-0

N-Boc-2-aminoacetaldehyde

Purity: 95%

Molecular weight: 159.18g/mol

Ref: 54-OR912671

N-Boc-2-aminoacetaldehyde (Technical Grade)

Controlled Product

CAS: 89711-08-0

Formula: C₇H₁₃NO₃

Color and Shape: Neat

Molecular weight: 159.18

Ref: TR-B600600

N-Boc-2-Aminoacetaldehyde

CAS: 89711-08-0

Formula: C₇H₁₃NO₃

Purity: 95.0%

Color and Shape: Liquid

Molecular weight: 159.185

Ref: 10-F302648

N-Boc-2-aminoacetaldehyde

CAS: 89711-08-0

N-Boc-2-aminoacetaldehyde is an aliphatic aldehyde that has been used in the synthesis of a number of bioactive molecules. It is synthesized by reacting an N-Boc amino acid with chloroform and hydrochloric acid. The reaction time is typically 2 hours at room temperature, although it can be decreased to 20 minutes if the temperature is increased to 60°C. The product can be purified using extraction or recrystallization methods. N-Boc-2-aminoacetaldehyde reacts with chloride ions to form phosphoranes, which are useful in clinical development as antimicrobial peptides. This compound also reacts with fluorine to form hydrogenated derivatives that have been shown to have neurokinin activity in animal models.

Formula: C₇H₁₃NO₃

Purity: Min. 95%

Color and Shape: Colorless Powder

Molecular weight: 159.18 g/mol

Ref: 3D-FN158109

N-Boc-2-aminoacetaldehyde

CAS: 89711-08-0

Formula: C₇H₁₃NO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 159.1830

Ref: IN-DA0035MR