Cas 153813-67-3,N,N-DIMETHYL-2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)-1-ETHYLENAMINE

153813-67-3

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Basic information

Product Name: N,N-DIMETHYL-2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)-1-ETHYLENAMINE
Synonyms: N,N-DIMETHYL-N-[2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)VINYL]AMINE;N,N-DIMETHYL-2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)-1-ETHYLENAMINE;dimethyl[(E)-2-(3-methyl-4-nitro-1,2-oxazol-5-yl)ethenyl]amine
CAS NO:153813-67-3
Molecular Formula: C8H11N3O3
Molecular Weight: 197.19
EINECS: N/A
Product Categories: N/A
Mol File: 153813-67-3.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: N,N-DIMETHYL-2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)-1-ETHYLENAMINE(CAS DataBase Reference)
NIST Chemistry Reference: N,N-DIMETHYL-2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)-1-ETHYLENAMINE(153813-67-3)
EPA Substance Registry System: N,N-DIMETHYL-2-(3-METHYL-4-NITRO-5-ISOXAZOLYL)-1-ETHYLENAMINE(153813-67-3)

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: 153813-67-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 153813-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,1 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153813-67:
(8*1)+(7*5)+(6*3)+(5*8)+(4*1)+(3*3)+(2*6)+(1*7)=133
133 % 10 = 3
So 153813-67-3 is a valid CAS Registry Number.

153813-67-3Upstream product

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153813-67-3Relevant academic research and scientific papers

Preparation and reactivity of [2-(3-methyl-4-nitro-isoxazol-5-yl)-vinyl]-amines

Dere, Ravindra,Monasterolo, Claudio,Moccia, Maria,Adamo, Mauro F.A.

, p. 7168 - 7171 (2015)

Herein, we report our investigation into the reactivity of 5-enamino-4-nitroisoxazoles. This study revealed that the title compounds, in spite of conjugation to the 4-nitroisoxazole, displayed similar reactivity to enamines, reacting with electrophiles to form new C-C, C-N, and C-Cl bonds.

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