Cas 79282-98-7,[2-(3-Bromo-phenyl)-indolizin-3-yl]-[3,5-dibromo-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid

79282-98-7

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Basic information

Product Name: [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3,5-dibromo-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid
Synonyms: [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3,5-dibromo-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid
CAS NO:79282-98-7
Molecular Formula:
Molecular Weight: 781.336
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: [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3,5-dibromo-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid(CAS DataBase Reference)
NIST Chemistry Reference: [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3,5-dibromo-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid(79282-98-7)
EPA Substance Registry System: [2-(3-Bromo-phenyl)-indolizin-3-yl]-[3,5-dibromo-4-(3-dipropylamino-propoxy)-phenyl]-methanone; compound with oxalic acid(79282-98-7)

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: 79282-98-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79282-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79282-98:
(7*7)+(6*9)+(5*2)+(4*8)+(3*2)+(2*9)+(1*8)=177
177 % 10 = 7
So 79282-98-7 is a valid CAS Registry Number.

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79282-98-7Relevant academic research and scientific papers

Research in indolizines series. Influence of substitution in the neighbourhood of ether function in butoprozine series

Rosseels,Peiren,Inion,et al.

, p. 581 - 588 (2007/10/02)

The authors prepared 2-alkyl or 2-aryl-3-(4-dialkylaminopropoxy-benzoyl)-indolizines with mono- or di-substitution in the ortho positions of the ether function. The substituents may be halogen atoms or methyl or methoxy groups. The 2-alkyl derivatives mon

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