Cas 916599-30-9,acetic acid 2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-(5-methyl-2,4-dioxo-3,4-dihydro-2<i>H</i>-pyrimidin-1-ylmethyl)-ethyl ester

916599-30-9

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Basic information

Product Name: acetic acid 2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-ethyl ester
Synonyms:
CAS NO:916599-30-9
Molecular Formula:
Molecular Weight: 544.604
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: acetic acid 2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: acetic acid 2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-ethyl ester(916599-30-9)
EPA Substance Registry System: acetic acid 2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl)-ethyl ester(916599-30-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 916599-30-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916599-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,5,9 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 916599-30:
(8*9)+(7*1)+(6*6)+(5*5)+(4*9)+(3*9)+(2*3)+(1*0)=209
209 % 10 = 9
So 916599-30-9 is a valid CAS Registry Number.

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916599-30-9Relevant academic research and scientific papers

Glycerol nucleoside triphosphates: Synthesis and polymerase substrate activities

Horhota, Allen T.,Szostak, Jack W.,McLaughlin, Larry W.

, p. 5345 - 5347 (2007/10/03)

The synthesis of (S)-glycerol nucleoside triphosphates (gNTPs) and the analysis of their substrate activities for enzymatic polymerization is described. NTPs with simplified carbohydrate backbones such as the tNTPs (α-L-threose-NTPs) are polymerase substr

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