Cas 1241908-39-3,5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione

1241908-39-3

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Basic information

Product Name: 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione
Synonyms: 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione
CAS NO:1241908-39-3
Molecular Formula:
Molecular Weight: 622.629
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: 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione(1241908-39-3)
EPA Substance Registry System: 5,6-dibenzyl-1-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione(1241908-39-3)

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: 1241908-39-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1241908-39-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,9,0 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1241908-39:
(9*1)+(8*2)+(7*4)+(6*1)+(5*9)+(4*0)+(3*8)+(2*3)+(1*9)=143
143 % 10 = 3
So 1241908-39-3 is a valid CAS Registry Number.

1241908-39-3Upstream product

1241908-39-3Downstream Products

1241908-42-8 5,6-dibenzyl-1-(β-D-galactopyranosyl)pyrimidine-2,4(1H,3H)-dione

1241908-39-3Relevant academic research and scientific papers

Synthesis and anti-hepatitis B activity of new substituted uracil and thiouracil glycosides

Abdel-Aal, Mohammed T.

experimental part, p. 797 - 805 (2012/01/13)

A number of N- and S-substituted uracil and thiouracil glycosides were synthesized by coupling reaction of 5,6-dibenzyle pyrimidine derivatives with the corresponding acetobromosugar. The synthesized compounds were tested for their antiviral activity agai

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