Cas 137017-43-7,4-Amino-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-3-oxy-1H-pyrimidin-2-one

137017-43-7

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Basic information

Product Name: 4-Amino-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-3-oxy-1H-pyrimidin-2-one
Synonyms:
CAS NO:137017-43-7
Molecular Formula:
Molecular Weight: 257.246
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-Amino-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-3-oxy-1H-pyrimidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-Amino-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-3-oxy-1H-pyrimidin-2-one(137017-43-7)
EPA Substance Registry System: 4-Amino-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-3-oxy-1H-pyrimidin-2-one(137017-43-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 137017-43-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 137017-43-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,1 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137017-43:
(8*1)+(7*3)+(6*7)+(5*0)+(4*1)+(3*7)+(2*4)+(1*3)=107
107 % 10 = 7
So 137017-43-7 is a valid CAS Registry Number.

137017-43-7Upstream product

838-07-3 5-methyldeoxycytidine

137017-43-7Downstream Products

137017-43-7Relevant academic research and scientific papers

Oxidation of Cytosine and 5-Methylcytosine Nucleosides and 5-Methyl-2'-deoxycytidine 5'-Monophosphate with Peroxosulfate Ions

Itahara, Toshio

, p. 1591 - 1594 (1991)

Reaction of 5-methylcytosine nucleosides and nucleotide with Na2S2O8 resulted in an oxidation of the 5-methyl group, while treatment of them and cytosine nucleosides with KHSO5 gave the corresponding N3-oxides.

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