Cas 312499-66-4,ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(4-thiomorpholinylmethyl)-1H-1,2,3-triazole-4-carboxylate

312499-66-4

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Basic information

Product Name: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(4-thiomorpholinylmethyl)-1H-1,2,3-triazole-4-carboxylate
Synonyms: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(4-thiomorpholinylmethyl)-1H-1,2,3-triazole-4-carboxylate
CAS NO:312499-66-4
Molecular Formula: C12H17N7O3S
Molecular Weight: 340.35824
EINECS: N/A
Product Categories: N/A

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-(4-thiomorpholinylmethyl)-1H-1,2,3-triazole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(4-thiomorpholinylmethyl)-1H-1,2,3-triazole-4-carboxylate(312499-66-4)
EPA Substance Registry System: ethyl 1-(4-amino-1,2,5-oxadiazol-3-yl)-5-(4-thiomorpholinylmethyl)-1H-1,2,3-triazole-4-carboxylate(312499-66-4)

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: 312499-66-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 312499-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,4,9 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 312499-66:
(8*3)+(7*1)+(6*2)+(5*4)+(4*9)+(3*9)+(2*6)+(1*6)=144
144 % 10 = 4
So 312499-66-4 is a valid CAS Registry Number.

312499-66-4Upstream product

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312499-66-4Relevant 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 (2007/10/03)

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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