Cas 161265-87-8,diethyl 6-hydroxy-6-methyl-2-phenyl-4-(phenylamino)-3-cyclohexene-1,3-dicarboxylate

161265-87-8

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Basic information

Product Name: diethyl 6-hydroxy-6-methyl-2-phenyl-4-(phenylamino)-3-cyclohexene-1,3-dicarboxylate
Synonyms: diethyl 6-hydroxy-6-methyl-2-phenyl-4-(phenylamino)-3-cyclohexene-1,3-dicarboxylate
CAS NO:161265-87-8
Molecular Formula:
Molecular Weight: 423.509
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: diethyl 6-hydroxy-6-methyl-2-phenyl-4-(phenylamino)-3-cyclohexene-1,3-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 6-hydroxy-6-methyl-2-phenyl-4-(phenylamino)-3-cyclohexene-1,3-dicarboxylate(161265-87-8)
EPA Substance Registry System: diethyl 6-hydroxy-6-methyl-2-phenyl-4-(phenylamino)-3-cyclohexene-1,3-dicarboxylate(161265-87-8)

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: 161265-87-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161265-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,2,6 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161265-87:
(8*1)+(7*6)+(6*1)+(5*2)+(4*6)+(3*5)+(2*8)+(1*7)=128
128 % 10 = 8
So 161265-87-8 is a valid CAS Registry Number.

161265-87-8Upstream product

161265-87-8Downstream Products

161265-87-8Relevant academic research and scientific papers

ARYLAMINATION OF 2,4-DIACETYL(DIETHOXYCARBONYL)-5-HYDROXY-5-METHYL-3-PHENYL(2-FURYL)-1-CYCLOHEXANONES

Sorokin, V. V.,Kuz'min, M. V.,Smirnova, N. S.,Kozhevnikova, N. I.,Kriven'ko, A. P.

, p. 562 - 565 (2007/10/02)

The arylamination of 2,4-diacetyl(diethoxycarbonyl)-5-hydroxy-5-methyl-3-phenyl(2-furyl)-1-cyclohexanones takes place with participation of the carbonyl group of the alicycle and retention or elimination of the hydroxyl function and leads to the formation

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