Cas 943735-86-2,3-benzoyl-4-(2-chlorophenyl)-7,7-dimethyl-2-(phenylamino)-7,8-dihydro-4H-chromen-5(6H)-one

943735-86-2

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Basic information

Product Name: 3-benzoyl-4-(2-chlorophenyl)-7,7-dimethyl-2-(phenylamino)-7,8-dihydro-4H-chromen-5(6H)-one
Synonyms:
CAS NO:943735-86-2
Molecular Formula:
Molecular Weight: 483.994
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: 3-benzoyl-4-(2-chlorophenyl)-7,7-dimethyl-2-(phenylamino)-7,8-dihydro-4H-chromen-5(6H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-benzoyl-4-(2-chlorophenyl)-7,7-dimethyl-2-(phenylamino)-7,8-dihydro-4H-chromen-5(6H)-one(943735-86-2)
EPA Substance Registry System: 3-benzoyl-4-(2-chlorophenyl)-7,7-dimethyl-2-(phenylamino)-7,8-dihydro-4H-chromen-5(6H)-one(943735-86-2)

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: 943735-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 943735-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,7,3 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 943735-86:
(8*9)+(7*4)+(6*3)+(5*7)+(4*3)+(3*5)+(2*8)+(1*6)=202
202 % 10 = 2
So 943735-86-2 is a valid CAS Registry Number.

943735-86-2Upstream product

943735-86-2Downstream Products

943735-86-2Relevant academic research and scientific papers

Reactivity of functionalized N, S-ketene acetal: Regioselective construction of tetrahydrobenzo[b]pyran and chromeno[2,3-b] quinoline derivatives

Li, Ming,Hou, Yan-Li,Wen, Li-Rong,Gong, Fu-Meng

, p. 8522 - 8532 (2010)

Regioselective synthesis of functionalized tetrahydrobenzo[b]pyrans has been developed by multicomponent reactions (MCRs) and tandem [3 + 3] annulations of β-benzoylthioacetanilides or β-(2-haloaroyl)thioacetanilides as valuable sources with aromatic alde

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