Cas 129700-44-3,3-((1r,4r)-4-(4-chlorophenyl)cyclohexyl)-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate

129700-44-3

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Basic information

Product Name: 3-((1r,4r)-4-(4-chlorophenyl)cyclohexyl)-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate
Synonyms: 3-((1r,4r)-4-(4-chlorophenyl)cyclohexyl)-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate
CAS NO:129700-44-3
Molecular Formula:
Molecular Weight: 408.881
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: 3-((1r,4r)-4-(4-chlorophenyl)cyclohexyl)-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: 3-((1r,4r)-4-(4-chlorophenyl)cyclohexyl)-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate(129700-44-3)
EPA Substance Registry System: 3-((1r,4r)-4-(4-chlorophenyl)cyclohexyl)-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate(129700-44-3)

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: 129700-44-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129700-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,0 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129700-44:
(8*1)+(7*2)+(6*9)+(5*7)+(4*0)+(3*0)+(2*4)+(1*4)=123
123 % 10 = 3
So 129700-44-3 is a valid CAS Registry Number.

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129700-44-3Relevant academic research and scientific papers

ANTIMALARIAL COMPOSITIONS AND USES THEREOF

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Paragraph 00222, (2018/04/12)

Provided herein are compounds, compositions and method of using thereof to treat or prevent malaria.

Process for the preparation of trans-2,3-disubstituted naphthoquinones

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Page/Page column 2, (2010/06/16)

The invention concerns a new process for the preparation of naphthoquinones, in particular an improved process for the preparation of 2,3-disubstituted 1,4-naphthoquinones, in the trans configuration.

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