CAS 317842-48-1

Formel: C13H15NO2

InChl: InChI=1S/C13H15NO2/c1-5-10-6-8-11(9-7-10)14-12(15)16-13(2,3)4/h1,6-9H,2-4H3,(H,14,15)

InChI Key: ZGJXAIOPBAMFSE-UHFFFAOYSA-N

SMILES: CC(C)(C)OC(=O)NC1=CC=C(C=C1)C#C

tert-Butyl (4-ethynylphenyl)carbamate

CAS: 317842-48-1

Formel: C₁₃H₁₅NO₂

Reinheit: 97%

Farbe und Form: Solid

Molekulargewicht: 217.2637

Ref: IN-DA00CQJL

tert-Butyl (4-ethynylphenyl)carbamate

CAS: 317842-48-1

tert-Butyl (4-ethynylphenyl)carbamate

Formel: C₁₃H₁₅NO₂

Reinheit: 95%

Molekulargewicht: 217.26

Ref: 54-OR77099

tert-Butyl (4-ethynylphenyl)carbamate

CAS: 317842-48-1

tert-Butyl (4-ethynylphenyl)carbamate

Formel: C₁₃H₁₅NO₂

Reinheit: 97%

Molekulargewicht: 217.26

Ref: IN-DG00830502

tert-Butyl (4-ethynylphenyl)carbamate

CAS: 317842-48-1

Reinheit: 97%

Farbe und Form: Solid

Molekulargewicht: 217.2680054

Ref: 10-F762817

tert-Butyl N-(4-ethynylphenyl)carbamate

CAS: 317842-48-1

Tert-butyl N-(4-ethynylphenyl)carbamate is a new chemical compound that is synthesized by the Sharpless 1,3-dipolar cycloaddition reaction. This novel method can be used to introduce the tert-butyl group into peptides and proteins in an efficient manner. Tert-butyl N-(4-ethynylphenyl)carbamate has been shown to react with histidine residues on the surface of proteins and peptides, which can be used for introducing reactive groups or eliminating side chains. The introduction of such groups can be useful in protein engineering.

Formel: C₁₃H₁₅NO₂

Reinheit: Min. 95%

Molekulargewicht: 217.26 g/mol

Ref: 3D-SMA84248