Cas 334024-82-7,5-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2<i>H</i>-pyrimidin-1-yl)-3-phenylselanyl-pyrrolidine-1-carboxylic acid <i>tert</i>-butyl ester

334024-82-7

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Basic information

Product Name: 5-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-phenylselanyl-pyrrolidine-1-carboxylic acid tert-butyl ester
Synonyms: 5-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-phenylselanyl-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS NO:334024-82-7
Molecular Formula:
Molecular Weight: 480.422
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-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-phenylselanyl-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-phenylselanyl-pyrrolidine-1-carboxylic acid tert-butyl ester(334024-82-7)
EPA Substance Registry System: 5-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-phenylselanyl-pyrrolidine-1-carboxylic acid tert-butyl ester(334024-82-7)

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: 334024-82-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 334024-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,0,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 334024-82:
(8*3)+(7*3)+(6*4)+(5*0)+(4*2)+(3*4)+(2*8)+(1*2)=107
107 % 10 = 7
So 334024-82-7 is a valid CAS Registry Number.

334024-82-7Upstream product

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334024-82-7Relevant academic research and scientific papers

Stereoselective synthesis of azanucleosides aza-stavudine (aza-D4T), aza-2′,3′-didehydro-3′-deoxyuridine (aza-D4U), and its hydrogenated analogues from an endocyclic enecarbamate

Costenaro, Edson R.,Fontoura, Luis A. M.,Oliveira, Denilson F.,Correia, Carlos R. D.

, p. 1599 - 1602 (2007/10/03)

The stereoselective synthesis of the aza-analogues of nucleosides stavudine (D4T) and dideoxyuridine (DDU) were accomplished in a very concise manner (3-4 step sequences) with high overall yields from a five-membered endocyclic enecarbamate employing phenylselenenyl bromide as an effective promoter.

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