52886-04-1 Usage
Physical state
Colorless liquid
Odor
Faint
Common uses
Monomer in the production of various polymers
Flammability
Highly flammable
Handling precautions
Should be handled with care
Use as building block
Synthesis of various organic compounds
Importance
Intermediate in the production of pharmaceuticals, agrochemicals, and fragrances
Industrial applications
Manufacture of resins, coatings, and adhesives
Polymerization ability
Forms durable materials
Potential
Renewable and sustainable bio-based building block for materials and chemicals
Check Digit Verification of cas no
The CAS Registry Mumber 52886-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52886-04:
(7*5)+(6*2)+(5*8)+(4*8)+(3*6)+(2*0)+(1*4)=141
141 % 10 = 1
So 52886-04-1 is a valid CAS Registry Number.
52886-04-1Relevant articles and documents
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Boland,W.,Jaenicke,L.
, p. 4819 - 4824 (1979)
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A short chemoenzymatic synthesis of (+)-Multifidene and (+)-Viridiene
Lebreton, Jacques,Alphand, Veronique,Furstoss, Roland
, p. 1011 - 1014 (2007/10/03)
(+)-Multifidene 1 and (+)-Viridiene 2, the major constituents of some brown algae pheromones, were synthesized in five steps from racemic bicycloheptenone 3 via a novel microbiological Baeyer-Villiger oxidation performed using the fungi Cunninghamella echinulata.
Synthesis of Cis Vicinally Disubstituted Cyclopentanes by Fragmentation of Bicycloheptan-6-ols. Total Synthesis of (+/-)-Multifidene
Burks, John E.,Crandall, Jack K.
, p. 4663 - 4670 (2007/10/02)
A fragmentation-olefination process has been developed for the conversion of bicycloheptan-6-ols bearing anion stabilizing functions at C-7 into cyclopentanes with vicinal and functionalized methyl substituents.Under appropriate conditions reasonab
