N~6~-[(Benzyloxy)carbonyl]-L-lysine

Basic Information

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CAS Number

1155-64-2

Molecular Formula

C14H20N2O4

Molecular Weight

280.32 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Ethers

Basic Chemical Raw Materials Organic Chemicals Amines

Fine Chemicals Dyes and Pigments Organic Dyes

Fine Chemicals Surfactants Anionic Surfactants

Basic Physical Properties

Physical State

White to Yellow Solid

Melting Point

259 °C (dec.)

Boiling Point

499.6℃ at 760 mmHg

Flash Point

255.9℃

Refractive Index

16 ° (C=1.6, 2mol/L HCl)

Specific Rotation

14.4 º (c=1.6 in 1N HCl)

SMILES

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C1=CC=C(C=C1)COC(=O)NCCCCC(C(=O)O)N

InChI

InChI=1S/C14H20N2O4/c15-12(13(17)18)8-4-5-9-16-14(19)20-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10,15H2,(H,16,19)(H,17,18)/t12-/m0/s1

InChIKey

CKGCFBNYQJDIGS-LBPRGKRZSA-N

LogP

1.4949999999999992

Topological Polar Surface Area

101.64999999999999 Å²

Hydrogen Bond Donor/Acceptor

4 / 6

Complexity

304

Safety Information

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Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation

H319 Causes serious eye irritation
Serious eye damage/eye irritation

H335 May cause respiratory irritation
Specific target organ toxicity, single exposure; Respiratory tract irritation

Hazard Class

Class IRRITANT Class IRRITANT

Synonyms & References

English

SCHEMBL453671
Nepsilon -benzyloxycarbonyl-L-lysine
9VC
(S)-2-Amino-6-(((benzyloxy)carbonyl)amino)hexanoic acid;H-Lys(Z)-OH
AKOS015924148
J-300184
N6-((Benzyloxy)carbonyl)-L-lysine
N .epsilon.-Z-L-Lysine
.epsilon.-Carbobenzoxy-L-lysine
HY-W007750
H-Lys(Z)
(2S)-2-amino-6-(phenylmethoxycarbonylamino)hexanoic acid
Nepsilon-Carbobenzoxy-L-lysine
N~6~-[(benzyloxy)carbonyl]-L-lysine
N6-Cbz-L-Lysine
N6-(Benzyloxycarbonyl)-L-lysine
EINECS 214-585-7
AM20050443
(2S)-2-azaniumyl-6-(phenylmethoxycarbonylamino)hexanoate
(2S)-2-amino-6-{[(benzyloxy)carbonyl]amino}hexanoic acid
.epsilon.-N-cbz-L-lysine
Lysine, N6-[(phenylmethoxy)carbonyl]-
AKOS005175147
n'-benzyloxycarbonyl-l-lysine
epsilon-Carbobenzoxy-L-lysine
N(6)-Carbobenzyloxy-l-lysine
N .epsilon.-Carbobenzyloxy-L-lysine
N6-Benzyloxycarbonyl-L-lysine
N(epsilon)-Carbobenzoxylysine
N-.epsilon.-cbz-L-lysine
6-N-benzyloxycarbonyl-lysine

MDL Number

MFCD00002638

FAQ

What is N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2)?

N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2) is a protected amino acid derivative used in chemical synthesis. Its chemical formula is C14H19N2O4, and it features a benzyloxy carbonyl (Boc) group attached to the N6 position of L-lysine. This compound is commonly employed as an intermediate in peptide chemistry due to its stability and controlled reactivity.

What are the main uses of N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2)?

N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2) is primarily used in pharmaceutical research for synthesizing peptides and proteins. It serves as a key building block in drug development, particularly in creating bioactive molecules. Additionally, it finds applications in industrial chemical processes and as a research reagent for studying amino acid modifications and functional group chemistry.

Is N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2) safe?

N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2) is generally considered safe when handled properly. However, it should be used with standard laboratory safety precautions, such as wearing gloves and ensuring adequate ventilation. While toxicity data is limited, it is recommended to follow OSHA guidelines and avoid prolonged skin contact or inhalation to ensure safe handling.

How should N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2) be stored?

N~6~-[(Benzyloxy)carbonyl]-L-lysine (CAS: 1155-64-2) should be stored in a cool, dry, and dark environment to maintain stability. It is best kept in a sealed container at 2-8°C to prevent moisture absorption and degradation. Avoid exposure to heat, humidity, or direct light to ensure long-term preservation and optimal performance in chemical reactions.