Cas 1407489-36-4,7-(diphenylmethylene)-7H-cyclopenta[1,2-b:4,3-b']dithiophene

1407489-36-4

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Basic information

Product Name: 7-(diphenylmethylene)-7H-cyclopenta[1,2-b:4,3-b']dithiophene
Synonyms: 7-(diphenylmethylene)-7H-cyclopenta[1,2-b:4,3-b']dithiophene
CAS NO:1407489-36-4
Molecular Formula:
Molecular Weight: 342.485
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: 7-(diphenylmethylene)-7H-cyclopenta[1,2-b:4,3-b']dithiophene(CAS DataBase Reference)
NIST Chemistry Reference: 7-(diphenylmethylene)-7H-cyclopenta[1,2-b:4,3-b']dithiophene(1407489-36-4)
EPA Substance Registry System: 7-(diphenylmethylene)-7H-cyclopenta[1,2-b:4,3-b']dithiophene(1407489-36-4)

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: 1407489-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1407489-36-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,4,8 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1407489-36:
(9*1)+(8*4)+(7*0)+(6*7)+(5*4)+(4*8)+(3*9)+(2*3)+(1*6)=174
174 % 10 = 4
So 1407489-36-4 is a valid CAS Registry Number.

1407489-36-4Upstream product

18592-86-4 2,2′-dibromo-[3,3′]bithiophene

1407489-36-4Downstream Products

1407489-36-4Relevant academic research and scientific papers

New synthesis of dibenzofulvenes by palladium-catalyzed double cross-coupling reactions

Shimizu, Masaki,Nagao, Ikuhiro,Kiyomoto, Shin-Ichi,Hiyama, Tamejiro

, p. 1277 - 1284,8 (2020/09/09)

Palladium-catalyzed double cross-coupling reactions of 1,1-bis(pinacolato) borylalk-1-enes with 2,2′-dibromobiaryls and of 9-stannafluorenes with 1,1-dibromoalk-1-enes have been demonstrated to serve as new synthetic methods for dibenzofulvenes.

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