N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(3-BENZOTHIENYL)-D-ALANINE
fmoc-3-(3-benzothienyl)-D-alanine
CAS: 177966-61-9
Molecular Formula: C26H21NO4S
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(3-BENZOTHIENYL)-D-ALANINE - Names and Identifiers
| Name | fmoc-3-(3-benzothienyl)-D-alanine |
| Synonyms | FMOC-D-BTA-OH RARECHEM BK PT 0208 Fmoc-D-3-Benzothienylala Fmoc-D-3-benzothienylalanine fmoc-β-(3-benzothienyl)-d-ala-oh Fmoc-D-3-(3-Benzothienyl)-alanine fmoc-3-(3-benzothienyl)-D-alanine Fmoc-beta-(3-benzothienyl)-D-Ala-OH N-ALPHA-FMOC-BETA-(3-BENZOTHIENYL)-D-ALANINE 3-Benzo[b]thiophen-3-yl-D-alanine, N-FMOC protected N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(3-BENZOTHIENYL)-D-ALANINE 3-(1-benzothiophen-3-yl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanine (R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(benzo[b]thiophen-3-yl)propanoic acid |
| CAS | 177966-61-9 |
| InChI | InChI=1/C26H21NO4S/c28-25(29)23(13-16-15-32-24-12-6-5-7-17(16)24)27-26(30)31-14-22-20-10-3-1-8-18(20)19-9-2-4-11-21(19)22/h1-12,15,22-23H,13-14H2,(H,27,30)(H,28,29)/t23-/m1/s1 |
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(3-BENZOTHIENYL)-D-ALANINE - Physico-chemical Properties
| Molecular Formula | C26H21NO4S |
| Molar Mass | 443.51 |
| Density | 1.356g/cm3 |
| Boling Point | 690.8°C at 760 mmHg |
| Flash Point | 371.6°C |
| Vapor Presure | 4.88E-20mmHg at 25°C |
| Storage Condition | Keep in dark place,Sealed in dry,2-8°C |
| Refractive Index | 1.687 |
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(3-BENZOTHIENYL)-D-ALANINE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| Hazard Class | IRRITANT |
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-(3-BENZOTHIENYL)-D-ALANINE - Introduction
fmoc-3-(3-benzothienyl)-D-alanine is a chiral amino acid with a structure similar to natural D-amino acids. Its main properties include:
1. Chiral amino acids: fmoc-3-(3-benzothienyl)-D-alanine is an unnatural amino acid, where Fmoc represents a benzyloxycarbonyl protecting group. The D-configuration indicates that its stereo configuration is dextrorotatory optically active.
2. It has a benzothiophene structure: fmoc-3-(3-benzothienyl)-D-alanine molecule also contains benzene ring and thiophene ring, which makes it have special optical and electrochemical properties.
The primary use of fmoc-3-(3-benzothienyl)-D-alanine is as a building block for the synthesis of biologically active polypeptides or proteins. It is used as an amino acid unit of the synthetic peptide chain in solid phase synthesis to synthesize polypeptides with specific biological activities or functions.
The preparation of fmoc-3-(3-benzothienyl)-D-alanine is usually carried out by means of chemical synthesis. Specifically, the chiral amino acid can be synthesized from the corresponding precursor compound through a series of chemical reactions, including the steps of protecting the hydroxyl group, replacing the benzyl group, etc.
Regarding safety information, fmoc-3-(3-benzothienyl)-D-alanine should be used and operated in accordance with the relevant safety technical instructions for chemicals. It can be irritating and dangerous to the eyes, skin and respiratory system. When in use, should wear appropriate protective equipment, avoid direct contact, avoid inhalation of aerosols or dust, and maintain good ventilation conditions. If necessary, professional advice should be sought.
1. Chiral amino acids: fmoc-3-(3-benzothienyl)-D-alanine is an unnatural amino acid, where Fmoc represents a benzyloxycarbonyl protecting group. The D-configuration indicates that its stereo configuration is dextrorotatory optically active.
2. It has a benzothiophene structure: fmoc-3-(3-benzothienyl)-D-alanine molecule also contains benzene ring and thiophene ring, which makes it have special optical and electrochemical properties.
The primary use of fmoc-3-(3-benzothienyl)-D-alanine is as a building block for the synthesis of biologically active polypeptides or proteins. It is used as an amino acid unit of the synthetic peptide chain in solid phase synthesis to synthesize polypeptides with specific biological activities or functions.
The preparation of fmoc-3-(3-benzothienyl)-D-alanine is usually carried out by means of chemical synthesis. Specifically, the chiral amino acid can be synthesized from the corresponding precursor compound through a series of chemical reactions, including the steps of protecting the hydroxyl group, replacing the benzyl group, etc.
Regarding safety information, fmoc-3-(3-benzothienyl)-D-alanine should be used and operated in accordance with the relevant safety technical instructions for chemicals. It can be irritating and dangerous to the eyes, skin and respiratory system. When in use, should wear appropriate protective equipment, avoid direct contact, avoid inhalation of aerosols or dust, and maintain good ventilation conditions. If necessary, professional advice should be sought.
Last Update：2024-04-09 20:02:46
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CAS: 177966-61-9
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CAS: 177966-61-9
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