Cas 113854-50-5,1-(4-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ<sup>2</sup>-triazoline

113854-50-5

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Basic information

Product Name: 1-(4-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ²-triazoline
Synonyms:
CAS NO:113854-50-5
Molecular Formula:
Molecular Weight: 319.32
EINECS: N/A
Product Categories: N/A
Mol File: 113854-50-5.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: 1-(4-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ²-triazoline(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ²-triazoline(113854-50-5)
EPA Substance Registry System: 1-(4-nitrophenyl)-3-ethoxycarbonyl-4-ethylideneamino-5-methyl-1,2,4-Δ²-triazoline(113854-50-5)

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: 113854-50-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113854-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,5 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113854-50:
(8*1)+(7*1)+(6*3)+(5*8)+(4*5)+(3*4)+(2*5)+(1*0)=115
115 % 10 = 5
So 113854-50-5 is a valid CAS Registry Number.

113854-50-5Upstream product

592-56-3 acetaldazine

113854-50-5Downstream Products

15966-46-8 1-(4-Nitro-phenyl)-5-methyl-1,2,4-triazol-carbonsaeure-(3)-aethylester

113854-50-5Relevant articles and documents

SYNTHESIS OF 1,2,4-TRIAZOLES AND 4-AMINO-1,2,4-Δ2-TRAIZOLINES ON THE BASIS OF AZINES AND NITRILE IMINES

Vasil'eva, L. P.,Akimova, G. S.,Chistokletov, V. N.

, p. 1776 - 1781 (2007/10/02)

The azines of benzaldehyde, 2-furaldehyde, and 3-phenylpropenal react with nitrile imines to form derivatives of 4-amino-1,2,4-Δ2-triazoline.Under the same conditions, depending on the structure of the nitrile imine, aliphatic aldazines give de

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