Cas 24706-53-4,1-(4-chlorophenyl)-6,6-dimethyl-1,5,6,7-tetrahydro-4H-benzo[d][1,2,3]triazol-4-one

24706-53-4

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Basic information

Product Name: 1-(4-chlorophenyl)-6,6-dimethyl-1,5,6,7-tetrahydro-4H-benzo[d][1,2,3]triazol-4-one
Synonyms: 1-(4-chlorophenyl)-6,6-dimethyl-1,5,6,7-tetrahydro-4H-benzo[d][1,2,3]triazol-4-one
CAS NO:24706-53-4
Molecular Formula:
Molecular Weight: 275.738
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: 1-(4-chlorophenyl)-6,6-dimethyl-1,5,6,7-tetrahydro-4H-benzo[d][1,2,3]triazol-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-chlorophenyl)-6,6-dimethyl-1,5,6,7-tetrahydro-4H-benzo[d][1,2,3]triazol-4-one(24706-53-4)
EPA Substance Registry System: 1-(4-chlorophenyl)-6,6-dimethyl-1,5,6,7-tetrahydro-4H-benzo[d][1,2,3]triazol-4-one(24706-53-4)

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: 24706-53-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 24706-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24706-53:
(7*2)+(6*4)+(5*7)+(4*0)+(3*6)+(2*5)+(1*3)=104
104 % 10 = 4
So 24706-53-4 is a valid CAS Registry Number.

24706-53-4Upstream product

24706-47-6 3-(4-chlorophenylamino)-5,5-dimethylcyclohex-2-enone

24706-53-4Downstream Products

24706-53-4Relevant academic research and scientific papers

Base-Promoted Synthesis of N-Substituted 1,2,3-Triazoles via Enaminone-Azide Cycloaddition Involving Regitz Diazo Transfer

Wan, Jie-Ping,Cao, Shuo,Liu, Yunyun

, p. 6034 - 6037 (2016)

The domino reactions between NH-based secondary enaminones and tosyl azide have been developed for the synthesis of various N-substituted 1,2,3-triazoles by employing t-BuONa as the base promoter. Through a key Regitz diazo-transfer process with tosyl azi

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