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10017-66-0

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10017-66-0 Usage

General Description

Pseudouridine is a naturally occurring isomer that is found in various substances, including wheat bran. It is considered a modified nucleoside that is present in different types of RNA, and contributes to the structure and function of RNA molecules. Pseudouridine contributes in stability, activity, and post-transcriptional modifications of RNA. Its presence in wheat bran is due to its ubiquity in the plant kingdom and its role in RNA. It is also used as a biomarker for diseases and in research on the microbiome, in addition to playing a role in biotechnology and pharmacology. It is not directly associated with any harmful effects and is generally seen as a positive element in nutrition and functionality. Some studies show it may have potential health benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 10017-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,1 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10017-66:
(7*1)+(6*0)+(5*0)+(4*1)+(3*7)+(2*6)+(1*6)=50
50 % 10 = 0
So 10017-66-0 is a valid CAS Registry Number.

10017-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name α-pseudouridine

1.2 Other means of identification

Product number -
Other names α-ψ-Uridin

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:10017-66-0 SDS

10017-66-0Downstream Products

10017-66-0Relevant articles and documents

A Synthesis of Pseudouridine

Brown, Daniel M.,Ogden, Richard C.

, p. 723 - 725 (2007/10/02)

2,3,5-Tri-O-benzylribose and 2,4-di-t-butoxy-5-lithiopyrimidine (from the 5-bromo-compound and butyllithium) in THF at -78 deg C give 5-(2,3,5-tri-O-benzyl-D-altro-pentahydroxypentyl)-2,4-di-t-butoxypyrimidine and its D-allo-epimer (ratio 5:2), which cyclise sterospecifically in ethanolic hydrochloric acid to 5-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)uracil and its α-anomer.Debenzylation by boron trichloride gives 5-β-D-ribofuranosyluracil, pseudouridine, and its α-anomer. 2,3,5-Tri-O-methylribose reacts analogously. 2,3-O-Isopropylideneribose and its 5-O-trityl derivative give no polyol, but instead 2,4-di-t-butoxy-5-(2-hydroxyisopropyl)pyrimidine.

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