Cas 134133-40-7,3-(1-Chloroethyl)-3,5-diphenyl-1,2-bis(isopropoxycarbonyl)-1,2,3,6-tetrahydro-6-methyl-1,2,4-triazine

134133-40-7

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Basic information

Product Name: 3-(1-Chloroethyl)-3,5-diphenyl-1,2-bis(isopropoxycarbonyl)-1,2,3,6-tetrahydro-6-methyl-1,2,4-triazine
Synonyms:
CAS NO:134133-40-7
Molecular Formula:
Molecular Weight: 486.011
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: 3-(1-Chloroethyl)-3,5-diphenyl-1,2-bis(isopropoxycarbonyl)-1,2,3,6-tetrahydro-6-methyl-1,2,4-triazine(CAS DataBase Reference)
NIST Chemistry Reference: 3-(1-Chloroethyl)-3,5-diphenyl-1,2-bis(isopropoxycarbonyl)-1,2,3,6-tetrahydro-6-methyl-1,2,4-triazine(134133-40-7)
EPA Substance Registry System: 3-(1-Chloroethyl)-3,5-diphenyl-1,2-bis(isopropoxycarbonyl)-1,2,3,6-tetrahydro-6-methyl-1,2,4-triazine(134133-40-7)

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: 134133-40-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 134133-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,3 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 134133-40:
(8*1)+(7*3)+(6*4)+(5*1)+(4*3)+(3*3)+(2*4)+(1*0)=87
87 % 10 = 7
So 134133-40-7 is a valid CAS Registry Number.

134133-40-7Upstream product

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134133-40-7Relevant academic research and scientific papers

Synthesis and Diastereofacial Selectivity in Diels-Alder Reactions of Halogenated 2-Aza 1,3-Dienes

Barluenga, Jose,Gonzalez, Francisco Javier,Fustero, Santos,Garcia-Granda, Santiago,Perez-Carreno, Enrique

, p. 4459 - 4463 (2007/10/02)

The synthesis of mono- and trihalogenated derivatives of 2-aza 1,3-dienes 2 and 3 is described.The first example of diastereofacial selectivity in Diels-Alder reactions of heterodienes of type 2 with electron-poor dienophiles is reported, and a model for

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