Cas 220323-15-9,(E)-3-(3,4-Dihydroxy-phenyl)-N-[(S)-1-methoxymethoxymethyl-2-((R)-methylsulfanylmethanesulfinyl)-ethyl]-acrylamide

220323-15-9

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Basic information

Product Name: (E)-3-(3,4-Dihydroxy-phenyl)-N-[(S)-1-methoxymethoxymethyl-2-((R)-methylsulfanylmethanesulfinyl)-ethyl]-acrylamide
Synonyms: (E)-3-(3,4-Dihydroxy-phenyl)-N-[(S)-1-methoxymethoxymethyl-2-((R)-methylsulfanylmethanesulfinyl)-ethyl]-acrylamide
CAS NO:220323-15-9
Molecular Formula:
Molecular Weight: 389.494
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: (E)-3-(3,4-Dihydroxy-phenyl)-N-[(S)-1-methoxymethoxymethyl-2-((R)-methylsulfanylmethanesulfinyl)-ethyl]-acrylamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(3,4-Dihydroxy-phenyl)-N-[(S)-1-methoxymethoxymethyl-2-((R)-methylsulfanylmethanesulfinyl)-ethyl]-acrylamide(220323-15-9)
EPA Substance Registry System: (E)-3-(3,4-Dihydroxy-phenyl)-N-[(S)-1-methoxymethoxymethyl-2-((R)-methylsulfanylmethanesulfinyl)-ethyl]-acrylamide(220323-15-9)

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: 220323-15-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220323-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,2 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 220323-15:
(8*2)+(7*2)+(6*0)+(5*3)+(4*2)+(3*3)+(2*1)+(1*5)=69
69 % 10 = 9
So 220323-15-9 is a valid CAS Registry Number.

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220323-15-9Relevant academic research and scientific papers

Synthesis and morphological reversion activity on src(ts)NRK cells of pyrimidinylpropanamide antibiotics, sparsomycin, sparoxomycin A1, A2, and their analogues

Nakajima, Noriyuki,Enomoto, Takeshi,Matsuura, Nobuyasu,Ubukata, Makoto

, p. 3331 - 3334 (2007/10/03)

Three pyrimidinylpropanamide antibiotics sparsomycin (1), sparoxomycins A1, A2 (2, 3), and also six analogues (4-9) have been synthesized by employing asymmetric sulfide oxidation conditions as a key step. Sparsomycin (1) and its alkyl analogues (5-7) showed higher morphological reversion activities on src(ts)NRK cells than 2 and 3.

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