BOC-3-D-ALA(2-FURYL)-OH DCHA

BOC-3-D-ALA(2-FURYL)-OH DCHA - Names and Identifiers

Name	(R)-N-BOC-2-Furylalanine
Synonyms	(R)-N-BOC-2-Furylalanine BOC-D-2-FURYLALANINE-DCHA Boc-D-2-Furylalanine-DCHA Boc-D-2-Furylalanine·DCHA Boc-3-(2-Furyl)-D-alanine BOC-D-ALA(2-FURYL)-OH DCHA BOC-3-D-ALA(2-FURYL)-OH DCHA Boc-D-2-Furylalanine Dcha Salt BOC-D-2-FURYLALANINE DCHA SALT boc-d-3-(2-furyl)-alanine·dcha N-tert-Butoxycarbonyl-2-furyl-D-alanine BOC-3-(2-FURYL)-D-ALANINE DICYCLOHEXYLAMINE SALT BOC-BETA-(2-FURYL)-D-ALANINE DICYCLOHEXYLAMMONIUM SALT (2R)-2-[(tert-butoxycarbonyl)amino]-3-furan-2-ylpropanoate (αR)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-furanpropanoic acid 2-[2-furanyl-[(2-methylpropan-2-yl)oxy-oxomethyl]amino]propanoic acid
CAS	261380-18-1
InChI	InChI=1/C12H17NO5/c1-12(2,3)18-11(16)13-9(10(14)15)7-8-5-4-6-17-8/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15)/p-1/t9-/m1/s1

BOC-3-D-ALA(2-FURYL)-OH DCHA - Physico-chemical Properties

Molecular Formula	C12H17NO5
Molar Mass	255.27
Density	1.207
Boling Point	398.5°C (rough estimate)
Flash Point	199.6°C
Vapor Presure	2.47E-07mmHg at 25°C
pKa	3.73±0.10(Predicted)
Storage Condition	2-8°C(protect from light)
Refractive Index	1.5300 (estimate)

BOC-3-D-ALA(2-FURYL)-OH DCHA - Risk and Safety

Hazard Symbols	Xi - Irritant
Safety Description	S24/25 - Avoid contact with skin and eyes.

BOC-3-D-ALA(2-FURYL)-OH DCHA - Introduction

(R)-N-BOC-2-Furylalanine, also known as (R)-N-BOC-2-Furylalanine, is a chiral compound. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: Usually a white crystalline solid.
-molecular formula: C14H19NO4
-Molecular weight: 265.31g/mol
-Melting point: about 135-138 degrees Celsius
-Solubility: Soluble in common solvents such as methanol, ethanol and dichloromethane.

Use:
- (R)-N-BOC-2-Furylalanine is an important amino acid derivative commonly used in organic synthesis. It can be used as chiral reagent and chiral intermediate in pharmaceutical and chemical fields.
-The compound can also be used to synthesize biologically active compounds, such as anti-tumor drugs, antibacterial drugs, etc.

Method:
-In General,(R)-N-BOC-2-Furylalanine can be synthesized by synthetic routes. A common synthetic method is the sulfuric acid catalyzed esterification of furfuryl alcohol and alanine, followed by protection with a N-BOC protecting group.

Safety Information:
- (R)-N-BOC-2-Furylalanine toxicity is low and there is no definite risk report.
-However, when using any chemical, strictly follow the safety procedures, avoid direct contact with skin and eyes, and ensure that the operation is carried out in a well-ventilated environment.

Last Update：2024-04-09 20:45:29