Cas 1329682-22-5,ethyl 5-((6-phenylbicyclo[3.1.0]hexan-6-yl)methylamino)-1-p-tolyl-1H-1,2,4-triazole-3-carboxylate

1329682-22-5

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Basic information

Product Name: ethyl 5-((6-phenylbicyclo[3.1.0]hexan-6-yl)methylamino)-1-p-tolyl-1H-1,2,4-triazole-3-carboxylate
Synonyms: ethyl 5-((6-phenylbicyclo[3.1.0]hexan-6-yl)methylamino)-1-p-tolyl-1H-1,2,4-triazole-3-carboxylate
CAS NO:1329682-22-5
Molecular Formula:
Molecular Weight: 416.523
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: ethyl 5-((6-phenylbicyclo[3.1.0]hexan-6-yl)methylamino)-1-p-tolyl-1H-1,2,4-triazole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-((6-phenylbicyclo[3.1.0]hexan-6-yl)methylamino)-1-p-tolyl-1H-1,2,4-triazole-3-carboxylate(1329682-22-5)
EPA Substance Registry System: ethyl 5-((6-phenylbicyclo[3.1.0]hexan-6-yl)methylamino)-1-p-tolyl-1H-1,2,4-triazole-3-carboxylate(1329682-22-5)

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: 1329682-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1329682-22-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,9,6,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1329682-22:
(9*1)+(8*3)+(7*2)+(6*9)+(5*6)+(4*8)+(3*2)+(2*2)+(1*2)=175
175 % 10 = 5
So 1329682-22-5 is a valid CAS Registry Number.

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1329682-22-5Relevant academic research and scientific papers

Reactivity of N-(1,2,4-triazolyl)-substituted 1,2,3-triazoles

Zibinsky, Mikhail,Fokin, Valery V.

, p. 4870 - 4872 (2011)

Synthetically useful rhodium(II) carbenes were obtained from N-(1,2,4-triazolyl)-substituted 1,2,3-triazoles and Rh(II) carboxylates. The electron-withdrawing 1,2,4-triazolyl group reveals the heretofore unknown reactivity of nonsulfonyl 1,2,3-triazoles, which exhibit the reactivity of diazo compounds. The resulting carbenes provide ready asymmetric access to secondary homoaminocyclopropanes (80-95% ee, dr >20:1) via reactions with olefins and also engage in efficient transannulation reactions with nitriles.

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