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7-Pentofuranosyl-7H-purin-6-amine, also known as 7-(β-D-ribofuranosyl)-7H-purin-6-amine, is a nucleoside composed of a purine base (adenine) attached to a pentose sugar (β-D-ribofuranose). 7-pentofuranosyl-7H-purin-6-amine is a key component of RNA (ribonucleic acid), where it plays a crucial role in the storage, replication, and expression of genetic information. The presence of adenine in RNA is essential for the proper functioning of various cellular processes, including protein synthesis and gene regulation. The chemical structure of 7-pentofuranosyl-7H-purin-6-amine is characterized by its glycosidic bond between the N1 position of adenine and the C1' position of the ribose sugar, forming a stable furanose ring. This specific arrangement is vital for the molecule's ability to participate in base pairing and other interactions within the RNA molecule.

485-08-5

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485-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 485-08-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 485-08:
(5*4)+(4*8)+(3*5)+(2*0)+(1*8)=75
75 % 10 = 5
So 485-08-5 is a valid CAS Registry Number.

485-08-5SDS

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 3-isatylidene acetone

1.2 Other means of identification

Product number -
Other names 3-acetonylidene-2-oxindole

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:485-08-5 SDS

485-08-5Downstream Products

485-08-5Relevant academic research and scientific papers

A reinvestigated mechanism of ribosylation of adenine under silylating conditions

Framski, Grzegorz,Gdaniec, Zofia,Gdaniec, Maria,Boryski, Jerzy

, p. 10123 - 10129 (2007/10/03)

The mechanism of chemical synthesis of adenosine has been reinvestigated. Depending on the reaction conditions and the presence of N6-protecting groups, ribosylation of adenine proceeds via different kinetic products: 3-riboadenine in strongly acidic media, 7-ribosylated derivative in the silyl method, and 1-(β-d-ribofuranosyl)adenine when applying N6-acyladenine and silylating conditions.

1,1,1,3,3,3-Hexafluoro-2-propanol for the Removal of the 4,4'-Dimethoxytrityl Protecting Group from the 5'-Hydroxyl of Acid-Sensitive Nucleosides and Nucleotides

Leonard, Nelson J.,Neelima

, p. 7833 - 7836 (2007/10/02)

1,1,1,3,3,3-Hexafluoro-2-propanol is introduced as a suitable reagent and solvent for the detritylation of 5'-O-(4,4'-dimethoxytrityl)-nucleosides and -deoxy- nucleosides, especially those that are susceptible to N-glycosyl cleavage under more strongly acidic conditions.

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