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Fmoc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid is a complex organic compound that is frequently utilized in the field of biochemistry, particularly for peptide synthesis. It is classified as an unusual amino acid due to its structural modifications that distinguish it from the 20 standard amino acids involved in protein formation. This molecule features a fluorophore group, which is essential for identification and tracking during biochemical reactions. The presence of a cyano-phenyl group in Fmoc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid enhances its fluorescence, making it valuable in applications that require significant light interaction and signal generation.

270065-90-2

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270065-90-2 Usage

Uses

Used in Biochemistry Research:
Fmoc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid is used as a research tool for its unique properties that allow it to interact with light and produce specific, identifiable signals. This makes it a crucial component in numerous scientific studies, particularly in the area of peptide synthesis.
Used in Fluorescence-based Applications:
In the field of fluorescence-based applications, Fmoc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid is used as a fluorescent marker for its ability to generate significant light signals. This property is particularly useful in applications that require the tracking and identification of specific biochemical reactions or processes.
Used in Drug Development:
Fmoc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid is employed in drug development as a building block for the synthesis of novel peptide-based therapeutics. Its unique structural features and fluorescence properties can be harnessed to create molecules with specific biological activities, potentially leading to the discovery of new drugs with improved efficacy and selectivity.
Used in Diagnostics:
In the diagnostics industry, Fmoc-(S)-3-Amino-4-(4-cyano-phenyl)-butyric acid is used as a diagnostic marker for its ability to produce fluorescence signals. This can be particularly useful in the development of assays and tests that rely on the detection of specific biochemical interactions or the presence of certain molecules in biological samples.

Check Digit Verification of cas no

The CAS Registry Mumber 270065-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,0,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 270065-90:
(8*2)+(7*7)+(6*0)+(5*0)+(4*6)+(3*5)+(2*9)+(1*0)=122
122 % 10 = 2
So 270065-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C26H22N2O4/c27-15-18-11-9-17(10-12-18)13-19(14-25(29)30)28-26(31)32-16-24-22-7-3-1-5-20(22)21-6-2-4-8-23(21)24/h1-12,19,24H,13-14,16H2,(H,28,31)(H,29,30)/t19-/m0/s1

270065-90-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-(S)-3-amino-4-(4-cyanophenyl)-butyric acid

1.2 Other means of identification

Product number -
Other names N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(4-CYANOPHENYL)BUTANOIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:270065-90-2 SDS

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