Cas 1054635-41-4,Benzoic acid (3aS,4R,6R,6aR)-6-methoxy-2,2-dimethyl-4-vinyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester

1054635-41-4

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Basic information

Product Name: Benzoic acid (3aS,4R,6R,6aR)-6-methoxy-2,2-dimethyl-4-vinyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester
Synonyms:
CAS NO:1054635-41-4
Molecular Formula:
Molecular Weight: 334.369
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: Benzoic acid (3aS,4R,6R,6aR)-6-methoxy-2,2-dimethyl-4-vinyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (3aS,4R,6R,6aR)-6-methoxy-2,2-dimethyl-4-vinyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester(1054635-41-4)
EPA Substance Registry System: Benzoic acid (3aS,4R,6R,6aR)-6-methoxy-2,2-dimethyl-4-vinyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester(1054635-41-4)

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: 1054635-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1054635-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,4,6,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1054635-41:
(9*1)+(8*0)+(7*5)+(6*4)+(5*6)+(4*3)+(3*5)+(2*4)+(1*1)=134
134 % 10 = 4
So 1054635-41-4 is a valid CAS Registry Number.

1054635-41-4Upstream product

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1054635-41-4Relevant academic research and scientific papers

Synthesis and cytotoxicity of 4-amino-5-oxopyrido[2,3-d]pyrimidine nucleosides

Girardet,Gunic,Esler,Cieslak,Pietrzkowski,Wang

, p. 3704 - 3713 (2000)

A number of nucleoside analogues have been either used clinically as anticancer drugs or evaluated in clinical studies, while new nucleoside analogues continue to show promise. In this article, we report synthesis and cytotoxicity of a series of new pyrid

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