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1013328-63-6

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  • N-α-(9-Fluorenylmethoxycarbonyl)-β-[acridine-9(10H)-on-2-yl]-L-alanine;N-α-(9-Fluorenylmethoxycarbonyl)-β-{2-[9(10H)-acridonyl]}-L-alanine

    Cas No: 1013328-63-6

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1013328-63-6 Usage

Classification

Amino Acid
It belongs to the class of amino acids, which are the building blocks of proteins.

Fluoren-9-ylmethoxycarbonylamino group

Aromatic compound derived from fluorene with a methoxycarbonyl (-OCH3) group attached to the amino (-NH2) functional group.

9-oxo-9,10-dihydroacridin-2-yl group

A heterocyclic compound with a 9-oxo (-C=O) group and a 9,10-dihydro (hydrogen atoms added to the ring) structure, derived from acridine.

Propionic acid molecule

A short-chain carboxylic acid (-COOH) with a three-carbon backbone.

Unique structure

The compound has a distinctive structure, with two different functional groups attached to the propionic acid molecule, which may contribute to its potential applications.

Potential applications

Medicinal chemistry and drug development
Due to its unique structure and properties, the compound may have potential uses in the field of medicinal chemistry and drug development.

Further research and testing

More studies and tests are needed to determine the specific uses and potential benefits of the compound in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1013328-63-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,3,3,2 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1013328-63:
(9*1)+(8*0)+(7*1)+(6*3)+(5*3)+(4*2)+(3*8)+(2*6)+(1*3)=96
96 % 10 = 6
So 1013328-63-6 is a valid CAS Registry Number.

1013328-63-6Downstream Products

1013328-63-6Relevant articles and documents

Minimalist probes for studying protein dynamics: Thioamide quenching of selectively excitable fluorescent amino acids

Goldberg, Jacob M.,Speight, Lee C.,Fegley, Mark W.,Petersson, E. James

, p. 6088 - 6091 (2012)

Fluorescent probe pairs that can be selectively excited in the presence of Trp and Tyr are of great utility in studying conformational changes in proteins. However, the size of these probe pairs can restrict their incorporation to small portions of a prot

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