Cas 180857-76-5,1,4-dimethyl-6-<(1H-indol-3-yl)methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione

180857-76-5

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Basic information

Product Name: 1,4-dimethyl-6-<(1H-indol-3-yl)methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione
Synonyms: 1,4-dimethyl-6-<(1H-indol-3-yl)methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione
CAS NO:180857-76-5
Molecular Formula:
Molecular Weight: 465.552
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: 1,4-dimethyl-6-<(1H-indol-3-yl)methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione(CAS DataBase Reference)
NIST Chemistry Reference: 1,4-dimethyl-6-<(1H-indol-3-yl)methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione(180857-76-5)
EPA Substance Registry System: 1,4-dimethyl-6-<(1H-indol-3-yl)methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione(180857-76-5)

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: 180857-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 180857-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,8,5 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 180857-76:
(8*1)+(7*8)+(6*0)+(5*8)+(4*5)+(3*7)+(2*7)+(1*6)=165
165 % 10 = 5
So 180857-76-5 is a valid CAS Registry Number.

180857-76-5Upstream product

180857-76-5Downstream Products

180857-78-7 1,4-dimethyl-6-<<(1-phenylmethoxycarbonyl)indol-3-yl>methyl>-3-<(3-phenylmethoxy)phenylmethylene>-(Z)-2,5-piperazinedione

180857-76-5Relevant academic research and scientific papers

Synthetic Studies on Thaxtomins A and B, Phytotoxins Associated with Streptomyces scabies, the Causal Organism of Potato Common Scab

Gelin, Jacques,Mortier, Jacques,Moyroud, Joel,Chene, Alain

, p. 3473 - 3475 (1993)

The preliminary results of a study on the stereocontrolled racemic synthesis of thaxtomins A and B are disclosed.The synthesis features a new C-C bond-forming reaction: dilithium tetrachlorocuprate was shown to be an efficient catalyst for cross-coupling

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