Cas 1007198-31-3,2-(N-trityl-1H-imidazol-4-yl)-7-acetoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan

1007198-31-3

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Basic information

Product Name: 2-(N-trityl-1H-imidazol-4-yl)-7-acetoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan
Synonyms: 2-(N-trityl-1H-imidazol-4-yl)-7-acetoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan
CAS NO:1007198-31-3
Molecular Formula:
Molecular Weight: 708.767
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-(N-trityl-1H-imidazol-4-yl)-7-acetoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan(CAS DataBase Reference)
NIST Chemistry Reference: 2-(N-trityl-1H-imidazol-4-yl)-7-acetoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan(1007198-31-3)
EPA Substance Registry System: 2-(N-trityl-1H-imidazol-4-yl)-7-acetoxy-6-methoxy-3-(3,4,5-trimethoxybenzoyl)benzo[b]furan(1007198-31-3)

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: 1007198-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007198-31-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,1,9 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1007198-31:
(9*1)+(8*0)+(7*0)+(6*7)+(5*1)+(4*9)+(3*8)+(2*3)+(1*1)=123
123 % 10 = 3
So 1007198-31-3 is a valid CAS Registry Number.

1007198-31-3Upstream product

1007198-31-3Downstream Products

1007198-31-3Relevant academic research and scientific papers

An efficient synthesis and substitution of 3-aroyl-2-bromobenzo[b]furans

Gill, Gurmit S.,Grobelny, Damian W.,Chaplin, Jason H.,Flynn, Bernard L.

, p. 1131 - 1134 (2008/09/18)

(Chemical Equation Presented) A convenient method for the synthesis of 2-bromo-3-aroyl-benzo[b]furans from readily accessible precursors has been developed. The 2-bromo group has been employed as a versatile synthetic handle in both palladium-mediated cou

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