Cas 477200-19-4,6-(tert-butyl-diphenyl-silanyloxymethyl)-6-methyl-5,6-dihydro-4H-pyrimidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester

477200-19-4

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Basic information

Product Name: 6-(tert-butyl-diphenyl-silanyloxymethyl)-6-methyl-5,6-dihydro-4H-pyrimidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester
Synonyms: 6-(tert-butyl-diphenyl-silanyloxymethyl)-6-methyl-5,6-dihydro-4H-pyrimidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester
CAS NO:477200-19-4
Molecular Formula:
Molecular Weight: 538.759
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: 6-(tert-butyl-diphenyl-silanyloxymethyl)-6-methyl-5,6-dihydro-4H-pyrimidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-(tert-butyl-diphenyl-silanyloxymethyl)-6-methyl-5,6-dihydro-4H-pyrimidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester(477200-19-4)
EPA Substance Registry System: 6-(tert-butyl-diphenyl-silanyloxymethyl)-6-methyl-5,6-dihydro-4H-pyrimidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester(477200-19-4)

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: 477200-19-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 477200-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,7,2,0 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 477200-19:
(8*4)+(7*7)+(6*7)+(5*2)+(4*0)+(3*0)+(2*1)+(1*9)=144
144 % 10 = 4
So 477200-19-4 is a valid CAS Registry Number.

477200-19-4Upstream product

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477200-19-4Relevant academic research and scientific papers

Enantioselective synthesis of the bromopyrrole alkaloids manzacidin A and C by stereospecific C-H bond oxidation

Wehn, Paul M.,Du Bois

, p. 12950 - 12951 (2007/10/03)

The manzacidins represent a small family of structurally unique secondary metabolites found only sparingly in nature. Efforts to probe the pharmacological profile of these intriguing bromopyrrole alkaloids have been precluded by a deficiency of available

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