Cas 141562-48-3,<R-<R*,S*-(E)>>-N-<1-(hydroxymethyl)-2-<<(benzylthio)methyl>sulfinyl>ethyl>-3-(1,2,3,4-tetrahydro-1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-2-propenamide

141562-48-3

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Basic information

Product Name: >-N-<1-(hydroxymethyl)-2-<<(benzylthio)methyl>sulfinyl>ethyl>-3-(1,2,3,4-tetrahydro-1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-2-propenamide
Synonyms: >-N-<1-(hydroxymethyl)-2-<<(benzylthio)methyl>sulfinyl>ethyl>-3-(1,2,3,4-tetrahydro-1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-2-propenamide
CAS NO:141562-48-3
Molecular Formula:
Molecular Weight: 465.594
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: >-N-<1-(hydroxymethyl)-2-<<(benzylthio)methyl>sulfinyl>ethyl>-3-(1,2,3,4-tetrahydro-1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-2-propenamide(CAS DataBase Reference)
NIST Chemistry Reference: >-N-<1-(hydroxymethyl)-2-<<(benzylthio)methyl>sulfinyl>ethyl>-3-(1,2,3,4-tetrahydro-1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-2-propenamide(141562-48-3)
EPA Substance Registry System: >-N-<1-(hydroxymethyl)-2-<<(benzylthio)methyl>sulfinyl>ethyl>-3-(1,2,3,4-tetrahydro-1,3,6-trimethyl-2,4-dioxo-5-pyrimidinyl)-2-propenamide(141562-48-3)

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: 141562-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141562-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 141562-48:
(8*1)+(7*4)+(6*1)+(5*5)+(4*6)+(3*2)+(2*4)+(1*8)=113
113 % 10 = 3
So 141562-48-3 is a valid CAS Registry Number.

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141562-48-3Relevant academic research and scientific papers

Synthesis of sparsomycin derivatives, addressing its binding to the large ribosomal subunit

Broek, L. A. G. M.,Antonisse, A. J. J. van den,Ottenheijm, H. C. J.,Felix, A. San,Lazaro, E.,et al.

, p. 163 - 169 (1992)

The syntheses of compounds 14-19, 6-methyluracilacryloyl derivatives, and 27-29, photoreactive aryl azide analogs of the antitumor antibiotic sparsomycin (1) are described.All of the modifications in the 6-methyluracilacryloyl part of 1 were achieved by s

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