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Cytosinine is a naturally occurring nucleoside, which is a derivative of the nucleobase cytosine. It is found in certain RNA molecules, particularly in the context of certain tRNAs, where it plays a role in the decoding of genetic information during protein synthesis. Cytosinine is formed by the attachment of cytosine to a ribose sugar, which is a component of RNA. It is not as common as other nucleosides like adenosine, guanosine, uridine, and thymidine, but it is significant for its specific functions in RNA biology. The presence of cytosinine can influence the structure and function of RNA, and it has been implicated in various biological processes, including the regulation of gene expression and the fidelity of protein synthesis.

1860-84-0

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1860-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1860-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1860-84:
(6*1)+(5*8)+(4*6)+(3*0)+(2*8)+(1*4)=90
90 % 10 = 0
So 1860-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N4O4/c11-5-1-2-7(18-8(5)9(15)16)14-4-3-6(12)13-10(14)17/h1-5,7-8H,11H2,(H,15,16)(H2,12,13,17)

1860-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-6-(4-amino-2-oxopyrimidin-1-yl)-3,6-dihydro-2H-pyran-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Cytosinine

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:1860-84-0 SDS

1860-84-0Upstream product

1860-84-0Downstream Products

1860-84-0Relevant academic research and scientific papers

A highly efficient, asymmetric synthesis of blastidic acid: The β-amino acid component of the antibiotic, (+)-blasticidin S

Bischoff, Roland,McDonald, Niall,Sutherland, Andrew

, p. 7147 - 7149 (2007/10/03)

A new approach for the asymmetric synthesis of blastidic acid, the β-amino acid component of the antibiotic, (+)-blasticidin S has been achieved in 11 steps and 30% overall yield. The key transformations involve a one-pot Swern/Wittig reaction sequence to

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