Cas 86716-31-6,N-(5-Ethyl-[1,3,4]thiadiazol-2-yl)-2-(5-p-tolyloxymethyl-[1,3,4]oxadiazol-2-ylsulfanyl)-acetamide

86716-31-6

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Basic information

Product Name: N-(5-Ethyl-[1,3,4]thiadiazol-2-yl)-2-(5-p-tolyloxymethyl-[1,3,4]oxadiazol-2-ylsulfanyl)-acetamide
Synonyms:
CAS NO:86716-31-6
Molecular Formula:
Molecular Weight: 391.475
EINECS: N/A
Product Categories: N/A
Mol File: 86716-31-6.mol
Article Data: 1

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: N-(5-Ethyl-[1,3,4]thiadiazol-2-yl)-2-(5-p-tolyloxymethyl-[1,3,4]oxadiazol-2-ylsulfanyl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-Ethyl-[1,3,4]thiadiazol-2-yl)-2-(5-p-tolyloxymethyl-[1,3,4]oxadiazol-2-ylsulfanyl)-acetamide(86716-31-6)
EPA Substance Registry System: N-(5-Ethyl-[1,3,4]thiadiazol-2-yl)-2-(5-p-tolyloxymethyl-[1,3,4]oxadiazol-2-ylsulfanyl)-acetamide(86716-31-6)

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: 86716-31-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86716-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,1 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86716-31:
(7*8)+(6*6)+(5*7)+(4*1)+(3*6)+(2*3)+(1*1)=156
156 % 10 = 6
So 86716-31-6 is a valid CAS Registry Number.

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86716-31-6Relevant articles and documents

Synthesis of some new substituted 1,3,4-oxadiazoles as potential insecticidal, antibacterial and anti-acetylcholine esterase agents

Misra

, p. 487 - 493 (1983)

A series of 5-substituted phenoxymethyl-2[N-(2-alkyl-1,3,4-thiadiazol-5-yl)carbamoylmethylthio]-1,3, 4-oxadiazoles have been synthesized. All compounds were tested for their insecticidal, antibacterial and anti-acetylcholine esterase activities. Most of t

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