Cas 1137536-90-3,5-[4,4-bis(hydroxymethyl)cyclohexyl]pyrimidine-2,4(1H,3H)-dione

1137536-90-3

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Basic information

Product Name: 5-[4,4-bis(hydroxymethyl)cyclohexyl]pyrimidine-2,4(1H,3H)-dione
Synonyms: 5-[4,4-bis(hydroxymethyl)cyclohexyl]pyrimidine-2,4(1H,3H)-dione
CAS NO:1137536-90-3
Molecular Formula:
Molecular Weight: 254.286
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: 5-[4,4-bis(hydroxymethyl)cyclohexyl]pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-[4,4-bis(hydroxymethyl)cyclohexyl]pyrimidine-2,4(1H,3H)-dione(1137536-90-3)
EPA Substance Registry System: 5-[4,4-bis(hydroxymethyl)cyclohexyl]pyrimidine-2,4(1H,3H)-dione(1137536-90-3)

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: 1137536-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1137536-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,7,5,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1137536-90:
(9*1)+(8*1)+(7*3)+(6*7)+(5*5)+(4*3)+(3*6)+(2*9)+(1*0)=153
153 % 10 = 3
So 1137536-90-3 is a valid CAS Registry Number.

1137536-90-3Upstream product

1137536-86-7 5-[4,4-bis(hydroxymethyl)cyclohex-1-enyl]-6-chloropyrimidine-2,4(1H,3H)-dione

1137536-90-3Downstream Products

1137536-90-3Relevant academic research and scientific papers

Two convergent approaches toward novel carbocyclic C-nucleosides

Nencka, Radim,Sala, Michal,Dejmek, Milan,Drainsky, Martin,Holy, Antonin,Hebabecky, Hubert

experimental part, p. 4119 - 4130 (2011/02/22)

Two convergent methodologies for construction of novel carbocyclic C-nucleosides allowing the syntheses of derivatives with uracil heterobase substituted at the position C-5 as well as C-6 were developed. The crucial step of the first methodology was the

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