CAS 846549-33-5

Formula: C11H20N4O4

InChI: InChI=1S/C11H20N4O4/c1-11(2,3)19-10(18)14-8(9(16)17)6-4-5-7-13-15-12/h8H,4-7H2,1-3H3,(H,14,18)(H,16,17)/t8-/m0/s1

InChI key: SKRPDWWWUARZIW-QMMMGPOBSA-N

SMILES: CC(C)(C)OC(=O)N[C@@H](CCCCN=[N+]=[N-])C(=O)O

Boc-ε-azido-Nle-OH · DCHA

CAS: 846549-33-5

Lysine-derived building block for “click chemistry” and other reactions involving azides. The azido moiety may also be selectively converted into an amino group with triphenylphosphine in the presence of water.

Formula: C₁₁H₂₀N₄O₄·C₁₂H₂₃N

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 453.63

Ref: 01-4072397

(2S)-6-Azido-2-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoic acid

CAS: 846549-33-5

(2S)-6-Azido-2-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoic acid

Formula: C₁₁H₂₀N₄O₄

Purity: 98%

Molecular weight: 272.3

Ref: 54-OR1106299

(2S)-6-Azido-2-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoic acid

CAS: 846549-33-5

Formula: C₁₁H₂₀N₄O₄

Purity: 98%

Color and Shape: Liquid

Molecular weight: 272.3009

Ref: IN-DA008H0E

(S)-6-Azido-2-((tert-butoxycarbonyl)amino)hexanoic acid

CAS: 846549-33-5

Formula: C₁₁H₂₀N₄O₄

Purity: 95%

Molecular weight: 272.3

Ref: IN-DG00824940

Boc-L-Lys(N3)-OH

CAS: 846549-33-5

Boc-L-Lys(N3)-OH is a click chemistry reagent containing an azido group. Click chemistry holds vast potential for enabling the conjugation of nucleic acids, lipids, proteins, and other molecules. Its widespread application across numerous research areas is attributed to beneficial features such as high yield, high specificity, and simplicity.

Formula: C₁₁H₂₀N₄O₄

Color and Shape: Solid

Molecular weight: 272.3

Ref: TM-T89712