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50885-12-6

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50885-12-6 Usage

General Description

1-Amino-3-methoxynaphthalene is a chemical compound with the molecular formula C11H11NO. It is a derivative of naphthalene with an amino group and a methoxy group attached to carbon atoms 1 and 3, respectively. 1-Amino-3-methoxynaphthalene is commonly used as a fluorescent dye in various biochemical and molecular biology applications, including staining and visualization of proteins and nucleic acids in gels and tissues. It has also been investigated for its potential use in organic electronics and optoelectronic devices due to its unique optical and electronic properties. 1-Amino-3-methoxynaphthalene is considered to be a hazardous chemical and should be handled and used with caution, following proper safety protocols and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 50885-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,8 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50885-12:
(7*5)+(6*0)+(5*8)+(4*8)+(3*5)+(2*1)+(1*2)=126
126 % 10 = 6
So 50885-12-6 is a valid CAS Registry Number.

50885-12-6Relevant articles and documents

INHIBITORS OF KRAS G12C PROTEIN AND USES THEREOF

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Paragraph 00301; 00302, (2021/12/28)

Provided are novel compounds useful as inhibitors of the KRAS protein, as well as pharmaceutical compositions comprising these compounds and methods of treatment by administration of these compounds or the pharmaceutical compositions.

Sulfonated diarylrhodamine dyes

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, (2008/06/13)

Sulfonated diarylrhodamine compounds are useful as fluorescent labels of nucleosides, nucleotides, polynucleotides, and polypeptides. The compounds find particular application in the area of fluorescent nucleic acid analysis, e.g., automated DNA sequencing and fragment analysis, detection of probe hybridization in hybridization arrays, detection of nucleic acid amplification products, and the like.

Dibenzorhodamine dyes

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, (2008/06/13)

Dibenzorhodamine compounds having the structure are disclosed, including nitogen- and aryl-substituted forms thereof. In addition, intermediates useful for synthesizing such compounds are disclosed, such intermediates having the structure In Formula I, R1 is H or wherein Y is H, lower alkyl, lower alkene, lower alkyne, aromatic, phenyl, polycyclic aromatic, heterocycle, water-solubilizing group, or linking group, including substituted forms thereof. When R1 is H, the C-12-bonded nitrogen and the C-12 and C-13 carbons form a first ring structure having from 4 to 7 members, and/or the C-12-bonded nitrogen and the C-11 and C-12 carbons form a second ring structure having from 5 to 7 members. The compounds of Formula I further include aryl- and nitrogen-substituted forms thereof. The invention further includes energy transfer dyes comprising the dibenzorhodamine compounds, nucleosides labeled with the dibenzorhodamine compounds, and nucleic acid analysis methods employing the dibenzorhodamine compounds.

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