Cas 203116-78-3,(Z)-2-[(E)-3-(2,6-Dichloro-phenyl)-acryloylamino]-3-dimethylamino-acrylic acid methyl ester

203116-78-3

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Basic information

Product Name: (Z)-2-[(E)-3-(2,6-Dichloro-phenyl)-acryloylamino]-3-dimethylamino-acrylic acid methyl ester
Synonyms: (Z)-2-[(E)-3-(2,6-Dichloro-phenyl)-acryloylamino]-3-dimethylamino-acrylic acid methyl ester
CAS NO:203116-78-3
Molecular Formula:
Molecular Weight: 343.21
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: (Z)-2-[(E)-3-(2,6-Dichloro-phenyl)-acryloylamino]-3-dimethylamino-acrylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-[(E)-3-(2,6-Dichloro-phenyl)-acryloylamino]-3-dimethylamino-acrylic acid methyl ester(203116-78-3)
EPA Substance Registry System: (Z)-2-[(E)-3-(2,6-Dichloro-phenyl)-acryloylamino]-3-dimethylamino-acrylic acid methyl ester(203116-78-3)

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: 203116-78-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 203116-78-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,1,1 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 203116-78:
(8*2)+(7*0)+(6*3)+(5*1)+(4*1)+(3*6)+(2*7)+(1*8)=83
83 % 10 = 3
So 203116-78-3 is a valid CAS Registry Number.

203116-78-3Upstream product

203116-78-3Downstream Products

203116-78-3Relevant academic research and scientific papers

Nitrosation of Methyl 2-Cinnamoylamino-3-dimethylamino-propenoates. Alkyl N-Cinnamoyloxalic Acid Hydroxyimidic Amides, Intermediates in the Synthesis of Alkyl 5-Styryl-1,2,4-oxadiazole-3-carboxylates

Kmetic, Matej,Stanovnik, Branko

, p. 1705 - 1708 (1997)

Alkyl 2-(substituted cinnamoylamino)-3-dimethylaminopropenoates 5, prepared either from glycine (1) and substituted cinnamoyl chlorides 2 via oxazol-5(4H)-ones 4, or from cinnamoylglycinate with t-butoxy-bisdimethylaminomethane, were transformed by nitros

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