FMOC-DAP(FMOC)-OH

FMOC-DAP(FMOC)-OH - Names and Identifiers

Name	Fmoc-Dap(Fmoc)-OH
Synonyms	Fmoc-Dap(Fmoc)-OH FMOC-DAP(FMOC)-OH RARECHEM EM WB 0112 N-ALPHA-N-BETA-BIS-FMOC-L-DIAMINOPROPIONIC ACID NALPHA,NBETA-DI-FMOC-L-2,3-DIAMINOPROPIONIC ACID N-ALPHA,BETA-BIS-FMOC-L-2,3-DIAMINOPROPIONIC ACID N-ALPHA,N-BETA-DI-FMOC-(S)-2,3-DIAMINOPROPIONIC ACID N-ALPHA,BETA-DI-FMOC-L-ALPHA,BETA-DIAMINOPROPIONIC ACID N-ALPHA, BETA-DI-(9-FLUORENYLMETHOXYCARBONYL)-L-DIAMINOPROPIONIC ACID N-ALPHA-N-BETA-BIS-(9-FLUORENYLMETHYLOXYCARBONYL)-L-2,3-DIAMINOPROPIONIC ACID N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-L-alanine
CAS	201473-90-7
InChI	InChI=1/C33H28N2O6/c36-31(37)30(35-33(39)41-19-29-26-15-7-3-11-22(26)23-12-4-8-16-27(23)29)17-34-32(38)40-18-28-24-13-5-1-9-20(24)21-10-2-6-14-25(21)28/h1-16,28-30H,17-19H2,(H,34,38)(H,35,39)(H,36,37)/t30-/m0/s1

FMOC-DAP(FMOC)-OH - Physico-chemical Properties

Molecular Formula	C33H28N2O6
Molar Mass	548.59
Density	1.330
Boling Point	809.5±65.0 °C(Predicted)
Flash Point	443.4°C
Vapor Presure	1.1E-27mmHg at 25°C
Appearance	Crystalline
Color	Off-white
pKa	3.53±0.10(Predicted)
Storage Condition	Sealed in dry,2-8°C
Refractive Index	1.649

FMOC-DAP(FMOC)-OH - Risk and Safety

WGK Germany	3
FLUKA BRAND F CODES	10
HS Code	29242990

FMOC-DAP(FMOC)-OH - Introduction

Fmoc-Dap(Fmoc)-OH is an organic compound containing fluorene and alanine moieties in its chemical structure.

In terms of properties, the compound is a white or slightly yellow powder with certain solubility. It is soluble in some organic solvents such as dimethyl sulfoxide and dichloromethane at room temperature. It is a chiral compound and can only exist in the form of L-alanine.

In Terms of Use, Fmoc-Dap(Fmoc)-OH is often used as a pharmaceutical intermediate. It can be used for the synthesis of specific drugs, especially drugs with aromatic ring structures.

Regarding the preparation method, the method for preparing Fmoc-Dap(Fmoc)-OH is relatively complicated, and a multi-step reaction is usually required. A commonly used synthetic method is the reaction of fluorenylmethoxycarbonyl-3-amino-propionic acid with N-fluorenylmethoxycarbonylacyl chloride to give the target product.

In terms of safety information, because the toxicity and danger of the compound are not specifically understood, more in-depth research and evaluation are needed. Appropriate safety precautions, including wearing protective gloves, goggles and protective clothing, are required when using and handling the compound, and ensuring that the operation is carried out in a well-ventilated laboratory environment.

Last Update：2024-04-10 22:30:50