220497-50-7
(S)-N-FMOC-2-(5-Bromothienyl)alanine
CAS: 220497-50-7
Molecular Formula: C22H18BrNO4S
220497-50-7 - Names and Identifiers
220497-50-7 - 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 |
220497-50-7 - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
220497-50-7 - 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.
(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
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Product Name: Fmoc-L-2-(5-Bromothienyl)alanine Request for quotationCAS: 220497-50-7
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Product Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromothiophen-2-yl)propanoic acid Visit Supplier Webpage Request for quotationCAS: 220497-50-7
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Product Name: Fmoc-L-2-(5-Bromothienyl)alanine Visit Supplier Webpage Request for quotationCAS: 220497-50-7
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Product Name: FMOC-L-2-(5-BROMOTHIENYL)ALANINE Visit Supplier Webpage Request for quotation
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CAS: 220497-50-7
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