Cas 1428087-52-8,diethyl 2-(2-formylphenyl)-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate

1428087-52-8

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Basic information

Product Name: diethyl 2-(2-formylphenyl)-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate
Synonyms: diethyl 2-(2-formylphenyl)-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate
CAS NO:1428087-52-8
Molecular Formula:
Molecular Weight: 376.406
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 2-(2-formylphenyl)-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: diethyl 2-(2-formylphenyl)-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate(1428087-52-8)
EPA Substance Registry System: diethyl 2-(2-formylphenyl)-4-hydroxy-4-methyl-6-oxocyclohexane-1,3-dicarboxylate(1428087-52-8)

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: 1428087-52-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1428087-52-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,0,8 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1428087-52:
(9*1)+(8*4)+(7*2)+(6*8)+(5*0)+(4*8)+(3*7)+(2*5)+(1*2)=168
168 % 10 = 8
So 1428087-52-8 is a valid CAS Registry Number.

1428087-52-8Upstream product

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1428087-52-8Relevant academic research and scientific papers

Catalysis by amberlyst A-21: A greener approach to 4,5,6,7-tetrahydro-1H- indazol-3(2H)-ones via construction of cyclohexanones

Rao, Manam Sreenivasa,Haritha, Meda,Kolli, Sunder Kumar,Basaveswara Rao, Mandava V.,Pal, Manojit

, p. 1076 - 1083 (2014)

The 4,5,6,7-tetrahydro-1H-indazol-3(2H)-one derivatives have been synthesized in good yields via a two-step method in a single pot. The initial step involved the construction of cyclohexanone ring from aromatic aldehydes and β-ketoester in i-PrOH using an

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