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2,6-Dioxa-3-azabicyclo[3.2.1]octane-5-methanol, 7-(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)-8-hydroxy-3-(phen oxyacetyl)-, (1R,5R,7R,8S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

847666-88-0

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847666-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847666-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,6,6 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 847666-88:
(8*8)+(7*4)+(6*7)+(5*6)+(4*6)+(3*6)+(2*8)+(1*8)=230
230 % 10 = 0
So 847666-88-0 is a valid CAS Registry Number.

847666-88-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2'-O,4'-C-(N-phenoxyacetylaminomethylene)uridine

1.2 Other means of identification

Product number -
Other names -

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:847666-88-0 SDS

847666-88-0Upstream product

847666-88-0Downstream Products

847666-88-0Relevant academic research and scientific papers

Design, synthesis, and properties of 2′,4′-BNANC: A bridged nucleic acid analogue

Rahman, S. M. Abdur,Seki, Sayori,Obika, Satoshi,Yoshikawa, Haruhisa,Miyashita, Kazuyuki,Imanishi, Takeshi

, p. 4886 - 4896 (2008/09/21)

The novel bridged nucleic-acid analogue 2′,4′-BNANC (2′-O,4′-C-aminomethylene bridged nucleic acid), containing a six-membered bridged structure with an N-O linkage, was designed and synthesized efficiently, demonstrating a one-pot intramolecul

Highly stable pyrimidine-motif triplex formation at physiological pH values by a bridged nucleic acid analogue

Rahman, S. M. Abdur,Seki, Sayori,Obika, Satoshi,Haitani, Sunao,Miyashita, Kazuyuki,Imanishi, Takeshi

, p. 4306 - 4309 (2008/03/11)

Good things come in threes: A novel bridged nucleic acid in which the furanose conformation was locked in the N form by a six-membered bridged moiety containing an N-O bond (see picture) has been developed. Triplex-forming oligonucleotides composed of thi

NOVEL ARTIFICIAL NUCLEIC ACIDS OF N-O BOND CROSSLINKAGE TYPE

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Page/Page column 16; 22, (2010/11/08)

It is intended to provide oligonucleotide analogs usable in, for exmaple, the antisense method which are highly tolerant to enzymes, have a strong and selective binding affinity for a single-stranded RNA and also are highly capable of forming a triple-str

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