Boc-D-Asp-Nh2 | CAS No. 200282-47-9

Boc-D-Asp-Nh2

Basic Information

View in Editor

CAS Number

200282-47-9

Molecular Formula

C9H16N2O5

Molecular Weight

232.24 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

Basic Physical Properties

SMILES

View in Editor

CC(C)(C)OC(=O)NC(CC(=O)O)C(=O)N

InChI

InChI=1S/C9H16N2O5/c1-9(2,3)16-8(15)11-5(7(10)14)4-6(12)13/h5H,4H2,1-3H3,(H2,10,14)(H,11,15)(H,12,13)/t5-/m1/s1

InChIKey

VKCARTLEXJLJBZ-RXMQYKEDSA-N

LogP

-0.1602999999999995

Topological Polar Surface Area

118.72000000000001 Å²

Hydrogen Bond Donor/Acceptor

4 / 7

Complexity

295

Synonyms & References

English

MFCD00151866
AKOS027327964
SCHEMBL11596489
FD21177
AS-48988
BOC-D-ASP-NH2
200282-47-9
Butanoic acid,4-amino-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-oxo-, (3R)-
Butanoic acid, 4-amino-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-oxo-, (3R)-
(3R)-4-amino-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoic acid
(3R)-3-{[(tert-butoxy)carbonyl]amino}-3-carbamoylpropanoic acid
DTXSID40426765
(R)-4-amino-3-(tert-butoxycarbonylamino)-4-oxobutanoic acid
(R)-4-Amino-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid
Boc-D-aspartic acid alpha-amide
Boc-D-aspartic acid α-amide
Boc-D-Asp-NH?
Boc-D-Asp-NH₂
CTK8F0136

MDL Number

MFCD00151866

FAQ

What are the physical and chemical properties of Boc-D-Asp-Nh2 (CAS: 200282-47-9)?

Boc-D-Asp-Nh2 is a protected amino acid derivative with a molecular weight of approximately 252.35 g/mol. Its crystalline form is white or off-white, and it is soluble in water. It exhibits moderate reactivity, particularly towards nucleophiles, and is commonly used in peptide synthesis and biophysical studies.

How is Boc-D-Asp-Nh2 (CAS: 200282-47-9) typically synthesized?

Boc-D-Asp-Nh2 is typically synthesized through a multi-step process involving the protection of the D-Asp carboxyl group with a Boc (tert-butoxycarbonyl) group. Commonly, this involves coupling a protected D-Asp with a Boc-activating reagent under standard peptide synthesis conditions, followed by deprotection of other groups as needed.

What industries use Boc-D-Asp-Nh2 (CAS: 200282-47-9)?

Boc-D-Asp-Nh2 is widely used in the pharmaceutical and biotechnology industries for the synthesis of peptides and proteins. It is also employed in polymer chemistry for the modification of polymers, and in sensor technology for detecting specific biological molecules. Its application in semiconductor fabrication is limited but may be used in certain specialized processes.

What precautions should be taken when handling Boc-D-Asp-Nh2 (CAS: 200282-47-9)?

When handling Boc-D-Asp-Nh2, it is important to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or under a fume hood. Spills should be disposed of according to safety data sheet (SDS) guidelines. Ensure proper storage in a cool, dry place, away from direct sunlight and heat sources.