Cas 1445973-82-9,(E)-3-(2-nitrophenyl)-1-(2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indol-3-yl)prop-2-en-1-one

1445973-82-9

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Basic information

Product Name: (E)-3-(2-nitrophenyl)-1-(2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indol-3-yl)prop-2-en-1-one
Synonyms: (E)-3-(2-nitrophenyl)-1-(2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indol-3-yl)prop-2-en-1-one
CAS NO:1445973-82-9
Molecular Formula:
Molecular Weight: 579.59
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-(2-nitrophenyl)-1-(2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indol-3-yl)prop-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(2-nitrophenyl)-1-(2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indol-3-yl)prop-2-en-1-one(1445973-82-9)
EPA Substance Registry System: (E)-3-(2-nitrophenyl)-1-(2-(2-nitrostyryl)-1-(phenylsulfonyl)-1H-indol-3-yl)prop-2-en-1-one(1445973-82-9)

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: 1445973-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1445973-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,9,7 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1445973-82:
(9*1)+(8*4)+(7*4)+(6*5)+(5*9)+(4*7)+(3*3)+(2*8)+(1*2)=199
199 % 10 = 9
So 1445973-82-9 is a valid CAS Registry Number.

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1445973-82-9Relevant academic research and scientific papers

Synthesis of calothrixins and its analogs using FeCl3-mediated domino reaction protocol

Ramalingam, Bose Muthu,Saravanan, Velu,Mohanakrishnan, Arasambattu K.

, p. 3726 - 3729 (2013/08/23)

A novel one pot synthesis of calothrixin B and its analogs is achieved involving an FeCl3-mediated domino reaction of enamines in dry DMF at reflux. Alternatively, the enamines upon interaction with CuBr2 in DMF at reflux led to the

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