Jump to content

Thymine: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
add zh link
Sango123 (talk | contribs)
m spacing
Line 1: Line 1:
<!-- Here is a table of data; skip past it to edit the text. -->
<!-- Here is a table of data; skip past it to edit the text. -->
<!-- <nowiki> Submit {{subst:chembox_simple_organic}} to get this template or go to [[Template:Chembox_simple_organic]]. </nowiki> -->
<!-- <nowiki> Submit {{subst:chembox_simple_organic}} to get this template or go to [[Template:Chembox_simple_organic]]. </nowiki> -->

{| border="1" cellpadding="2" cellspacing="0" align="right" style="margin-left:1em"
{| border="1" cellpadding="2" cellspacing="0" align="right" style="margin-left:1em"
! colspan="2" align=center bgcolor="#cccccc" | '''Thymine'''
! colspan="2" align=center bgcolor="#cccccc" | '''Thymine'''

Revision as of 03:05, 2 July 2005

Thymine
Chemical name 5-Methylpyrimidine-2,4(1H,3H)-dione
Chemical formula C5H6N2O2
Molecular mass 126.11 g/mol
Melting point 316 - 317 °C
CAS number 65-71-4
SMILES CC1=CNC(NC1=O)=O
Chemical structure of thymine

Thymine, also known as 5-methyluracil, is a pyrimidine nucleobase. It is found in the nucleic acid DNA. In RNA thymine is replaced with uracil. Thymine can base pair with adenine.

Thymine combined with deoxyribose creates the nucleoside thymidine. Thymidine can be phosphorylated with one, two or three phosphoric acid groups, creating respectively TMP, TDP or TTP (thymidine mono- di- or triphosphate).