Cas 270063-70-2,4-methyl-1-[1-(1-methoxyethyl)-2-methyl-2-propenyl]-2-(2-oxo-2-phenylethyl)1,2,4-triazolidine-3,5-dione

270063-70-2

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Basic information

Product Name: 4-methyl-1-[1-(1-methoxyethyl)-2-methyl-2-propenyl]-2-(2-oxo-2-phenylethyl)1,2,4-triazolidine-3,5-dione
Synonyms: 4-methyl-1-[1-(1-methoxyethyl)-2-methyl-2-propenyl]-2-(2-oxo-2-phenylethyl)1,2,4-triazolidine-3,5-dione
CAS NO:270063-70-2
Molecular Formula:
Molecular Weight: 345.398
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: 4-methyl-1-[1-(1-methoxyethyl)-2-methyl-2-propenyl]-2-(2-oxo-2-phenylethyl)1,2,4-triazolidine-3,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-1-[1-(1-methoxyethyl)-2-methyl-2-propenyl]-2-(2-oxo-2-phenylethyl)1,2,4-triazolidine-3,5-dione(270063-70-2)
EPA Substance Registry System: 4-methyl-1-[1-(1-methoxyethyl)-2-methyl-2-propenyl]-2-(2-oxo-2-phenylethyl)1,2,4-triazolidine-3,5-dione(270063-70-2)

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: 270063-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 270063-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,0,6 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 270063-70:
(8*2)+(7*7)+(6*0)+(5*0)+(4*6)+(3*3)+(2*7)+(1*0)=112
112 % 10 = 2
So 270063-70-2 is a valid CAS Registry Number.

270063-70-2Upstream product

70-11-1 α-bromoacetophenone

270063-70-2Downstream Products

270063-70-2Relevant academic research and scientific papers

Direct amination of olefins through sequential triazolinedione ene reaction and carbanion-assisted cleavage of the N-N urazole bond

Adam, Waldemar,Pastor, Aurelia,Wirth, Thomas

, p. 1295 - 1297 (2000)

(formula presented) Allylic amines 5 are obtained in 30-55% overall yields by the base-catalyzed hydrolysis of trialkylated allylic urazoles 3; the latter are prepared by the TAD ene reaction of the appropriate olefin and further N-alkylation with α-bromo

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