FMOC-L-2-(5-BROMOTHIENYL)ALANINE

FMOC-L-2-(5-BROMOTHIENYL)ALANINE - Names and Identifiers

Name	(S)-N-FMOC-2-(5-Bromothienyl)alanine
Synonyms	Fmoc-L-2-(5-Bromothienyl)Alanine FMOC-L-2-(5-BROMOTHIENYL)ALANINE (S)-N-FMOC-2-(5-Bromothienyl)alanine Fmoc-3-(5-bromothien-2-yl)-L-alanine (S)-N-FMOC-2-(5-BROMOTHIENYL)ALANINE FMoc-3-(5-broMothien-2-yl)-L-alanine (S)-N-fmoc-2-(5-Bromothienyl)alanine(e.e.) N-(9-Fluorenylmethoxycarbonyl)-5-bromo-2-thienyl-L-alanine N-(9-FLUORENYLMETHOXYCARBONYL)-5-BROMO-2-THIENYL-L-ALANINE N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-BETA-(5-BROMOTHIENYL)-L-ALANINE 3-(5-bromothiophen-2-yl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine (αS)-5-Bromo-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-thiophenepropanoic acid (2S)-3-(5-bromothiophen-2-yl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate (2S)-3-(5-bromothiophen-2-yl)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid
CAS	220497-50-7
InChI	InChI=1/C22H18BrNO4S/c23-20-10-9-13(29-20)11-19(21(25)26)24-22(27)28-12-18-16-7-3-1-5-14(16)15-6-2-4-8-17(15)18/h1-10,18-19H,11-12H2,(H,24,27)(H,25,26)/t19-/m0/s1

FMOC-L-2-(5-BROMOTHIENYL)ALANINE - Physico-chemical Properties

Molecular Formula	C22H18BrNO4S
Molar Mass	472.35
Density	1.4650 (estimate)
Melting Point	150.4 °C
Boling Point	657.9°C at 760 mmHg
Flash Point	351.7°C
Vapor Presure	3.31E-18mmHg at 25°C
Storage Condition	2-8°C(protect from light)
Refractive Index	1.662

FMOC-L-2-(5-BROMOTHIENYL)ALANINE - Risk and Safety

Safety Description

24/25 - Avoid contact with skin and eyes.

FMOC-L-2-(5-BROMOTHIENYL)ALANINE - Introduction

(S)-N-FMOC-2-(5-Bromothienyl)alanine, also known as (S)-N-FMOC-2-(5-Bromothienyl)alanine, is an organic compound. It is a compound containing a bromothiophene group and an alanine residue.

(S)-N-FMOC-2-(5-Bromothienyl)alanine is commonly used in solid-state synthesis and biochemistry. It can be used as an amino acid protecting group to protect the carboxyl group of amino acids in the synthesis of polypeptides and proteins. It can also serve as a building block for fluorescent labels and receptor molecules.

(S)-N-FMOC-2-(5-Bromothienyl)alanine is often prepared by organic synthesis methods. A typical synthetic method is to esterify 5-bromothiophene-2-carboxylic acid with L-alanine, and then protect the carboxyl group of the product as Fmoc group.

Regarding safety information,(S)-N-FMOC-2-(5-Bromothienyl)alanine has limited data. However, as an organic compound, it should usually be handled with caution. During use, appropriate personal protective equipment should be worn and operated in well-ventilated laboratory conditions. In addition, specific safety information should refer to the relevant safety data sheet.

Last Update：2024-04-09 20:52:54