Cas 6433-42-7,1,2-dimethylcyclohexene-4,5-trans-dicarboxylic acid

6433-42-7

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Basic information

Product Name: 1,2-dimethylcyclohexene-4,5-trans-dicarboxylic acid
Synonyms:
CAS NO:6433-42-7
Molecular Formula:
Molecular Weight: 198.219
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: 1,2-dimethylcyclohexene-4,5-trans-dicarboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-dimethylcyclohexene-4,5-trans-dicarboxylic acid(6433-42-7)
EPA Substance Registry System: 1,2-dimethylcyclohexene-4,5-trans-dicarboxylic acid(6433-42-7)

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: 6433-42-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 6433-42-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6433-42:
(6*6)+(5*4)+(4*3)+(3*3)+(2*4)+(1*2)=87
87 % 10 = 7
So 6433-42-7 is a valid CAS Registry Number.

6433-42-7Upstream product

6433-42-7Downstream Products

5680-10-4 4,5-dimethylphthalic acid

6433-42-7Relevant academic research and scientific papers

Highly-functionalized arene synthesis based on palladium on carbon-catalyzed aqueous dehydrogenation of cyclohexadienes and cyclohexenes

Yasukawa, Naoki,Yokoyama, Hiroki,Masuda, Masahiro,Monguchi, Yasunari,Sajiki, Hironao,Sawama, Yoshinari

supporting information, p. 1213 - 1217 (2018/03/28)

Transition metal-catalyzed dehydrogenation is a clean oxidation method requiring no additional oxidants. We have accomplished a heterogeneous Pd/C-catalyzed aqueous dehydrogenation of 1,4-cyclohexadienes and cyclohexenes to give the corresponding highly-functionalized arenes. Furthermore, various arenes could be efficiently constructed in a one-pot manner via a Diels-Alder reaction and the following dehydrogenation.

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