Cas 1027982-25-7,Acetic acid 2-(2,4-dioxo-6-phenyl-3,4-dihydro-2H-thieno[2,3-d]pyrimidin-1-ylmethoxy)-ethyl ester

1027982-25-7

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Basic information

Product Name: Acetic acid 2-(2,4-dioxo-6-phenyl-3,4-dihydro-2H-thieno[2,3-d]pyrimidin-1-ylmethoxy)-ethyl ester
Synonyms:
CAS NO:1027982-25-7
Molecular Formula:
Molecular Weight: 360.39
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-(2,4-dioxo-6-phenyl-3,4-dihydro-2H-thieno[2,3-d]pyrimidin-1-ylmethoxy)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 2-(2,4-dioxo-6-phenyl-3,4-dihydro-2H-thieno[2,3-d]pyrimidin-1-ylmethoxy)-ethyl ester(1027982-25-7)
EPA Substance Registry System: Acetic acid 2-(2,4-dioxo-6-phenyl-3,4-dihydro-2H-thieno[2,3-d]pyrimidin-1-ylmethoxy)-ethyl ester(1027982-25-7)

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: 1027982-25-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027982-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,9,8 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1027982-25:
(9*1)+(8*0)+(7*2)+(6*7)+(5*9)+(4*8)+(3*2)+(2*2)+(1*5)=157
157 % 10 = 7
So 1027982-25-7 is a valid CAS Registry Number.

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1027982-25-7Relevant academic research and scientific papers

Synthesis of Cyclic and Acyclic Nucleoside Analogues Having a Thiophene or Dihydrothiophene Ring Fused to the d Side of an Uracil

Jourdan, Fabrice,Renault, Jacques,Karamat, Abdesselam,Ladurie, Daniel,Robba, Max

, p. 953 - 958 (2007/10/02)

Synthesis of cyclic and acyclic nucleosides was achieved by alkylation of various new aglycones following the Vorbrueggen and Niedballa's procedure .The analytical results allowed us to conclude that the alkylation ocurred on N1 site led to the β anomeric form for the cyclic nucleosides.

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