Search results
Results from the WOW.Com Content Network
A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. [1] Due to the moderate dielectric constant of CXB (ε = 7.9 [2]), PMMA acquires charges that can be screened by the addition of salt (e.g. tetrabutyl ammonium bromide), leading to a very good approximation of colloidal hard sphere. [3]
Multiple double bonds take the form -diene, -triene, etc., with the size prefix of the chain taking an extra "a": CH 2 =CHCH=CH 2 is buta-1,3-diene. Simple cis and trans isomers may be indicated with a prefixed cis-or trans-: cis-but-2-ene, trans-but-2-ene. However, cis-and trans-are relative descriptors.
The 3 substrates of this enzyme are cis-1,2-dihydroxy-4-methylcyclohexa-3,5-diene-1-carboxylate, NAD +, and NADP +, whereas its 4 products are 4-methylcatechol, NADH, NADPH, and CO 2. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-CH group of donor with NAD+ or NADP+ as acceptor. The systematic name of ...
Other names in common use include cis-benzene glycol dehydrogenase, cis-1,2-dihydrocyclohexa-3,5-diene (nicotinamide adenine, and dinucleotide) oxidoreductase. This enzyme participates in 4 metabolic pathways : gamma-hexachlorocyclohexane degradation , toluene and xylene degradation , naphthalene and anthracene degradation , and styrene ...
With cycloheptene, the cis-isomer is always assumed but the trans-isomer does also exist. One procedure for the organic synthesis of trans-cycloheptene is by singlet photosensitization of cis-cycloheptene with methyl benzoate and ultraviolet light at −35 °C. [2] The double bond in the trans isomer is very strained. [3]
cis-1,2-Dihydrocatechol is the organic compound with the formula C 6 H 6 (OH) 2. Several isomers exist with this formula. It is a colorless solid melting near room temperature. The compound is classified as a 1,3-cyclohexadiene. It arises by the dihydroxylation of benzene catalyzed by toluene dioxygenase.
Enoyl-CoA-(∆) isomerase (EC 5.3.3.8, also known as dodecenoyl-CoA-(∆) isomerase, 3,2-trans-enoyl-CoA isomerase, ∆3(cis),∆2(trans)-enoyl-CoA isomerase, or acetylene-allene isomerase, [1] is an enzyme that catalyzes the conversion of cis- or trans-double bonds of coenzyme A (CoA) bound fatty acids at gamma-carbon (position 3) to trans double bonds at beta-carbon (position 2) as below:
Thus, the two substrates of this enzyme are cis-3-phenylcyclohexa-3,5-diene-1,2-diol and NAD +, whereas its 3 products are biphenyl-2,3-diol, NADH, and H +. This enzyme belongs to the family of oxidoreductases , specifically those acting on the CH-CH group of donor with NAD+ or NADP+ as acceptor.