CAS 150806-61-4

N-[(1,1-Dimethylethoxy)carbonyl]-N-phenylglycine

Description:

N-[(1,1-Dimethylethoxy)carbonyl]-N-phenylglycine, with the CAS number 150806-61-4, is an organic compound characterized by its structure, which includes a phenyl group and a glycine moiety. This compound features a dimethylethoxycarbonyl protecting group, which is commonly used in organic synthesis to protect amine functionalities during chemical reactions. The presence of the phenyl group contributes to its hydrophobic characteristics, while the glycine component provides polar characteristics due to the amino and carboxylic acid functional groups. This compound is typically utilized in peptide synthesis and other organic reactions where selective protection of functional groups is necessary. Its solubility is influenced by the balance between the hydrophobic phenyl group and the polar glycine structure. Additionally, it may exhibit specific reactivity patterns typical of amino acids and their derivatives, making it valuable in medicinal chemistry and the development of pharmaceuticals. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

Formula: C₁₃H₁₇NO₄

InChI: InChI=1S/C13H17NO4/c1-13(2,3)18-12(17)14(9-11(15)16)10-7-5-4-6-8-10/h4-8H,9H2,1-3H3,(H,15,16)

InChI key: InChIKey=KIAPYAZGXJCKQL-UHFFFAOYSA-N

SMILES: N(C(OC(C)(C)C)=O)(CC(O)=O)C1=CC=CC=C1

Synonyms:

• N-[(1,1-Dimethylethoxy)carbonyl]-N-phenylglycine
• [[(1,1-Dimethylethoxy)carbonyl]phenylamino]acetic acid
• 2-[[(tert-Butoxy)carbonyl](phenyl)amino]acetic acid
• Glycine, N-[(1,1-dimethylethoxy)carbonyl]-N-phenyl-
• N-(tert-Butoxycarbonyl)-N-phenylglycine

2-([(tert-Butoxy)carbonyl](phenyl)amino)acetic acid

CAS: 150806-61-4

Formula: C₁₃H₁₇NO₄

Purity: 97%

Molecular weight: 251.2784

Ref: IN-DA00HXTN

N-BOC-N-PHENYLGLYCINE

CAS: 150806-61-4

Formula: C₁₃H₁₇NO₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 251.282

Ref: 10-F386321

2-{[(tert-butoxy)carbonyl](phenyl)amino}acetic acid

CAS: 150806-61-4

2-{[(tert-Butoxy)carbonyl](phenyl)amino}acetic acid is a supramolecular building block that can be used as an additive for the synthesis of taxol, quinine and other drugs. The synthesis of 2-{[(tert-butoxy)carbonyl](phenyl)amino}acetic acid starts from the imine, which is generated by reaction with tert-butanol in the presence of a catalytic amount of pyridine. The imine is then dehydrated to form 2-{[(tert-butoxy)carbonyl](phenyl)amino}acetic acid. This method has been shown to be efficient and provides an asymmetric route to various pharmaceuticals.
2-[(tert-Butoxy)carbonyl]phenylaminoacetic acid was first synthesized in 1990 by Atsushi Ochiai and Yoshih

Formula: C₁₃H₁₇NO₄

Purity: Min. 95%

Molecular weight: 251.3 g/mol

Ref: 3D-AGA80661