Cas 870246-06-3,Carbamic acid, [2-[(2-ethyl-6-methylphenyl)amino]-1-(2-furanylmethyl)-2-oxoethyl]-, 1,1-dimethylethyl ester

870246-06-3

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Basic information

Product Name: Carbamic acid, [2-[(2-ethyl-6-methylphenyl)amino]-1-(2-furanylmethyl)-2-oxoethyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:870246-06-3
Molecular Formula: C21H28N2O4
Molecular Weight: 372.464
EINECS: N/A
Product Categories: N/A

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: Carbamic acid, [2-[(2-ethyl-6-methylphenyl)amino]-1-(2-furanylmethyl)-2-oxoethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [2-[(2-ethyl-6-methylphenyl)amino]-1-(2-furanylmethyl)-2-oxoethyl]-, 1,1-dimethylethyl ester(870246-06-3)
EPA Substance Registry System: Carbamic acid, [2-[(2-ethyl-6-methylphenyl)amino]-1-(2-furanylmethyl)-2-oxoethyl]-, 1,1-dimethylethyl ester(870246-06-3)

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: 870246-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 870246-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,2,4 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 870246-06:
(8*8)+(7*7)+(6*0)+(5*2)+(4*4)+(3*6)+(2*0)+(1*6)=163
163 % 10 = 3
So 870246-06-3 is a valid CAS Registry Number.

870246-06-3Upstream product

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870246-06-3Relevant academic research and scientific papers

Preparation and root growth-inhibitory activity of N-substituted 2-(2-chloroacetamido)-3-(furan-2-yl)propanamides

Kitagawa, Tokujiro,Asada, Makoto

, p. 1183 - 1189 (2005)

A series of N-substituted 2-(2-chloroacetamido)-3-(furan-2-yl)propanamides (16-18) was prepared through the reaction of chloroacetyl chloride with N-substituted 2-amino-3-(furan-2-yl)propanamides (15), which were obtained via condensation of 2-(tert-butox

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