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2H-1-Benzopyran-2-one, 7-[3-[bis(4-methoxyphenyl)phenylmethoxy]-2-hydroxypropoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

180344-44-9

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180344-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180344-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,3,4 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 180344-44:
(8*1)+(7*8)+(6*0)+(5*3)+(4*4)+(3*4)+(2*4)+(1*4)=119
119 % 10 = 9
So 180344-44-9 is a valid CAS Registry Number.

180344-44-9Relevant academic research and scientific papers

Non-nucleosidic coumarin derivatives as polynucleotide-crosslinking agents

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Page column 15, (2010/02/08)

Novel coumarin derivatives comprising a coumarin moiety linked to a non-nucleosidic backbone moiety are disclosed. The resulting molecules are typically used as photoactivate crosslinking groups when incorporated into polynucleotides as replacements for o

Nucleic acid sequence detection employing probes comprising non-nucleosidic coumarin derivatives as polynucleotide-crosslinking agents

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, (2008/06/13)

Methods and compositions are provided for detecting nucleic acid sequences. Probes comprising a crosslinking agent are combined with a sample which may comprise a target sequence which is complementary to the probe. Hybridization is allowed to occur between complementary sequences. The crosslinking agent is activated. Covalent bonds are formed between the probe and the target sequence if they are hybridized to one another. The crosslinked nucleic acids can then be detected to indicate the presence of the target sequence. Also provided are kits comprising reagents.

Non-nucleosidic coumarin derivatives as polynucleotide-crosslinking agents

-

, (2008/06/13)

Novel coumarin derivatives comprising a coumarin moiety linked to a non-nucleosidic backbone moiety are disclosed. The resulting molecules are typically used as photoactivate cross-linking groups when incorporated into polynucleotides as replacements for

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