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[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name) is a complex chiral molecule that features a tetrahydrofuran ring, a dihydropyrimidinyl group, and a diphosphate moiety. As a derivative of pyrimidine and a sugar phosphate, [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name) has multiple asymmetric carbon atoms, indicating its chiral nature. Although its precise biological function is not specified in the name, its structure hints at possible roles in metabolic pathways or as a substrate for enzymatic reactions. The non-preferred name suggests that there may be alternative nomenclature or preferred naming conventions for [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name).

1955-26-6

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1955-26-6 Usage

Uses

Used in Pharmaceutical Industry:
[(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name) could be used as a pharmaceutical agent for [specific medical condition or treatment] due to its unique structure and potential interactions with biological molecules.
Used in Biochemical Research:
In the field of biochemical research, [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name) may serve as a valuable tool for studying enzymatic reactions or metabolic pathways, given its pyrimidine and sugar phosphate components.
Used in Chemical Synthesis:
Due to its complex structure, [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl (2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl dihydrogen diphosphate (non-preferred name) could be utilized in the synthesis of other complex organic molecules, potentially leading to the development of new drugs or materials.

Check Digit Verification of cas no

The CAS Registry Mumber 1955-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1955-26:
(6*1)+(5*9)+(4*5)+(3*5)+(2*2)+(1*6)=96
96 % 10 = 6
So 1955-26-6 is a valid CAS Registry Number.

1955-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name UDP-β-L-rhamnose

1.2 Other means of identification

Product number -
Other names [[(2R,3S,4R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl] hydrogen phosphate

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:1955-26-6 SDS

1955-26-6Synthetic route

O5'-<2-α-D-glucopyranosyloxy-1,2-dihydroxy-diphosphoryl>-uridine

O5'-<2-α-D-glucopyranosyloxy-1,2-dihydroxy-diphosphoryl>-uridine

diphosphoric acid-1-β-L-rhamnopyranosyl ester-2-uridin-5'-yl ester
1955-26-6

diphosphoric acid-1-β-L-rhamnopyranosyl ester-2-uridin-5'-yl ester

Conditions
ConditionsYield
mit Hilfe von Enzym-Praeparaten aus den Blaettern von Phaseolus aureus;
mit Hilfe von Enzym-Praeparaten aus den Blaettern von Nicotiana tabacum;

1955-26-6Upstream product

1955-26-6Downstream Products

1955-26-6Relevant academic research and scientific papers

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