288617-76-5

288617-76-5 - Names and Identifiers

Name	Fmoc-alpha-allyl-D-alanine
Synonyms	Fmoc-alpha-All-L-Ala-OH (R)-N-FMOC-Α-ALLYLALANINE FMoc-α-Me-D-Gly(Allyl)-OH Fmoc-alpha-allyl-D-alanine (R)-N-Fmoc-alpha-allylalanine Fmoc-alpha-methyl-D-allylglycine (R)-N-Fmoc-2-(2'-propenyl)alanine (R)-N-FMOC-2-(2'-PROPYLENYL)ALANINE (R)-N-Fmoc-2-(2'-propylenyl)alanine (R)-N-Fmoc-2-(2'-Propylenyl)Alanine (R)-N-(9-Fluorenylmethylcarbamate)-2-(2'-propylenyl)alanine (2R)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-4-pentenoic acid (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-methylpent-4-enoic acid
CAS	288617-76-5
InChI	InChI=1S/C21H21NO4/c1-3-12-21(2,19(23)24)22-20(25)26-13-18-16-10-6-4-8-14(16)15-9-5-7-11-17(15)18/h3-11,18H,1,12-13H2,2H3,(H,22,25)(H,23,24)/t21-/m1/s1

288617-76-5 - Physico-chemical Properties

Molecular Formula	C21H21NO4
Molar Mass	351.4
Density	1.224
Boling Point	564.3±45.0 °C(Predicted)
Flash Point	295.054 °C
Appearance	liquid
Color	pale yellow
pKa	3.81±0.11(Predicted)
Storage Condition	Inert atmosphere,Store in freezer, under -20°C

288617-76-5 - Risk and Safety

Hazard Symbols	N - Dangerous for the environment
Risk Codes	50 - Very Toxic to aquatic organisms
Safety Description	61 - Avoid release to the environment. Refer to special instructions / safety data sheets.
TSCA	No

288617-76-5 - Introduction

Fmoc-alpha-allyl-D-alanine(Fmoc-alpha-allyl-D-alanine) is an organic compound. The following is an introduction to some of its properties, uses, methods and safety information:

Nature:
-Appearance: White to off-white solid
-molecular formula: C24H23NO4
-Molecular weight: 389.45g/mol
-Melting point: 125-130 ° C
-Solubility: Slightly soluble in water, soluble in organic solvents such as dimethyl sulfoxide (DMSO), ethanol and formic acid

Use:
Fmoc-alpha-allyl-D-alanine is a commonly used amino acid derivative, which is widely used in biomedical research and drug synthesis. It is commonly used for polypeptide synthesis in solid phase synthesis. This compound reacts with other amino acids through its α-amino group to form an extension of the peptide chain.

Method:
Fmoc-alpha-allyl-D-alanine synthesis methods are usually achieved through organic synthesis. A common method is to react α-allyl-D-alanine with N-fluorenecylimide (Fmoc-NH-OH) to form Fmoc-alpha-allyl-D-alanine.

Safety Information:
Fmoc-alpha-allyl-D-alanine are generally relatively safe under normal conditions of use. However, as an organic compound, it should be treated with caution and appropriate laboratory safety measures should be taken when using it. It is recommended to wear appropriate personal protective equipment, such as lab gloves and eye protection. In case of accidental exposure or discomfort, seek medical assistance immediately.

Last Update：2024-04-09 20:45:29