Cas 296771-71-6,ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(2,3-dihydro-1H-indol-1-ylmethyl)-1H-1,2,3-triazole-4-carboxylate

296771-71-6

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Basic information

Product Name: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(2,3-dihydro-1H-indol-1-ylmethyl)-1H-1,2,3-triazole-4-carboxylate
Synonyms: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(2,3-dihydro-1H-indol-1-ylmethyl)-1H-1,2,3-triazole-4-carboxylate
CAS NO:296771-71-6
Molecular Formula: C16H17N7O3
Molecular Weight: 355.35128
EINECS: N/A
Product Categories: N/A
Mol File: 296771-71-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(2,3-dihydro-1H-indol-1-ylmethyl)-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(2,3-dihydro-1H-indol-1-ylmethyl)-1H-1,2,3-triazole-4-carboxylate(296771-71-6)
EPA Substance Registry System: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(2,3-dihydro-1H-indol-1-ylmethyl)-1H-1,2,3-triazole-4-carboxylate(296771-71-6)

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: 296771-71-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 296771-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 296771-71:
(8*2)+(7*9)+(6*6)+(5*7)+(4*7)+(3*1)+(2*7)+(1*1)=196
196 % 10 = 6
So 296771-71-6 is a valid CAS Registry Number.

296771-71-6Upstream product

296771-71-6Downstream Products

296771-71-6Relevant academic research and scientific papers

Nucleophilic substitution in the series of (1,2,3-triazol-1-yl)-1,2,5- oxadiazoles. Reactions with N-, O-, and S-nucleophiles

Rozhkov,Batog,Struchkova

, p. 1923 - 1934 (2005)

Methods for the synthesis of amino(1,2,3-triazol-1-yl)-1,2,5-oxadiazoles (aminotriazolylfurazans) with CH2Cl and COCH2Br substituents in the triazole ring were developed and nucleophilic substitution for their halogen atom in reactio

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