Cas 91809-82-4,4-Cyclohexene-1,2-dicarboxylic acid, 4-(1-hydroxycyclohexyl)-, dimethyl ester

91809-82-4

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Basic information

Product Name: 4-Cyclohexene-1,2-dicarboxylic acid, 4-(1-hydroxycyclohexyl)-, dimethyl ester
Synonyms:
CAS NO:91809-82-4
Molecular Formula: C16H24O5
Molecular Weight: 296.364
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: 4-Cyclohexene-1,2-dicarboxylic acid, 4-(1-hydroxycyclohexyl)-, dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Cyclohexene-1,2-dicarboxylic acid, 4-(1-hydroxycyclohexyl)-, dimethyl ester(91809-82-4)
EPA Substance Registry System: 4-Cyclohexene-1,2-dicarboxylic acid, 4-(1-hydroxycyclohexyl)-, dimethyl ester(91809-82-4)

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: 91809-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91809-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,8,0 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91809-82:
(7*9)+(6*1)+(5*8)+(4*0)+(3*9)+(2*8)+(1*2)=154
154 % 10 = 4
So 91809-82-4 is a valid CAS Registry Number.

91809-82-4Upstream product

91809-82-4Downstream Products

91809-82-4Relevant academic research and scientific papers

TWO SIX-MEMBERED RINGS ANNELATION TO CYCLIC KETONES THROUGH TWO SEQUENTIAL DIELS-ALDER REACTIONS

Tsuge, Otohiko,Wada, Eiji,Kanemasa, Shuji,Sakoh, Hirohiko

, p. 709 - 712 (1984)

A method for the two six-membered rings annelation to cyclic ketones through two sequential Diels-Alder reactions is presented.Naphtho-annelated cycloalkanes with a variety of unsaturation are accessible by choosing the kind of dienophiles, the order of their use, and dehydrogenation.

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