Cas 432003-61-7,2-{4-[(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)methyl]phenoxy}-N-(4-methylphenyl)acetamide

432003-61-7

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Basic information

Product Name: 2-{4-[(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)methyl]phenoxy}-N-(4-methylphenyl)acetamide
Synonyms: 2-{4-[(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)methyl]phenoxy}-N-(4-methylphenyl)acetamide
CAS NO:432003-61-7
Molecular Formula: C25H19NO4
Molecular Weight: 397.42266
EINECS: N/A
Product Categories: N/A
Mol File: 432003-61-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-{4-[(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)methyl]phenoxy}-N-(4-methylphenyl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-{4-[(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)methyl]phenoxy}-N-(4-methylphenyl)acetamide(432003-61-7)
EPA Substance Registry System: 2-{4-[(1,3-dioxo-1,3-dihydro-2H-inden-2-ylidene)methyl]phenoxy}-N-(4-methylphenyl)acetamide(432003-61-7)

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: 432003-61-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 432003-61-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,2,0,0 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 432003-61:
(8*4)+(7*3)+(6*2)+(5*0)+(4*0)+(3*3)+(2*6)+(1*1)=87
87 % 10 = 7
So 432003-61-7 is a valid CAS Registry Number.

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432003-61-7Relevant academic research and scientific papers

Indole macrocycles formed by diindolylmethane ring closure

Purwono, Bambang,Kumar, Naresh,Black, David StC

, (2022/02/14)

Indole containing macrocyclic compounds can be formed from suitable diindolyl diesters and diamides by acidcatalysed reaction with formaldehyde to generate a 2,2′-linkage in the ring closure step. The alternative protocol in which macrocyclisation is attempted by lactone or lactam formation from starting 2,2′- diindolylmethane systems was unsuccessful in our examples.

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