63621-96-5 Usage
Description
(2Z,4Z)-HEXA-2,4-DIENE-1,6-DIOL, a colorless and odorless liquid, is a chemical compound classified under the diene alcohols. It is widely recognized for its versatility in organic chemistry, particularly due to its ability to participate in Diels-Alder reactions, making it a valuable building block for synthesizing a variety of organic compounds.
Uses
Used in Pharmaceutical Industry:
(2Z,4Z)-HEXA-2,4-DIENE-1,6-DIOL is used as a key intermediate for the production of various pharmaceuticals. Its role in the synthesis process is crucial, as it contributes to the development of new drugs and medicines that address a range of health conditions.
Used in Fragrance Industry:
In the fragrance industry, (2Z,4Z)-HEXA-2,4-DIENE-1,6-DIOL serves as a vital component in the creation of diverse scents. Its chemical properties allow for the development of unique and complex aromas, enhancing the sensory experience of consumers.
Used in Polymer Industry:
(2Z,4Z)-HEXA-2,4-DIENE-1,6-DIOL is utilized as a precursor in the synthesis of polymers, which are essential materials in various applications, including plastics, coatings, and adhesives. Its contribution to the polymer industry is significant, as it helps in the development of innovative and improved polymeric materials.
Used as a Precursor in Chemical Synthesis:
(2Z,4Z)-HEXA-2,4-DIENE-1,6-DIOL is also used as a precursor in the synthesis of other chemicals, highlighting its importance in the broader field of chemical manufacturing. Its ability to participate in Diels-Alder reactions makes it a versatile and valuable compound for creating a wide array of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 63621-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,2 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63621-96:
(7*6)+(6*3)+(5*6)+(4*2)+(3*1)+(2*9)+(1*6)=125
125 % 10 = 5
So 63621-96-5 is a valid CAS Registry Number.
63621-96-5Relevant articles and documents
Efficient Synthesis of Unsaturated Seven-membered Rings by an Entropy/Strain Reduction Strategy: 2,7-Dihydro-1H-azepines, -oxepines, -thiepines, -1H-phosphepine and 1,3-Cycloheptadienes
Walsh, James G.,Furlong, Patrick J.,Gilheany, Declan G.
, p. 67 - 68 (1994)
Substituted (Z,Z)-1,6-dibromohexa-2,4-dienes, obtained from substituted catechols via the corresponding diols, react with primary amines, lithium sulfide, sodium phenylphosphide and malonic ester enolate under mild conditions to give efficient syntheses of 2,7-dihydro-1H-azepines, 2,7-dihydrothiepines, 2,7-dihydro-1H-phosphepine and cyclohepta-1,3-dienes respectively while the precursor diols yield the 2,7-dihydrooxepines on treatment with toluene-p-sulfonyl chloride.
An oxidation and ring contraction approach to the synthesis of (±)-1-deoxynojirimycin and (±)-1-deoxyaltronojirimycin
Bagal, Sharan K.,Davies, Stephen G.,Lee, James A.,Roberts, Paul M.,Russell, Angela J.,Scott, Philip M.,Thomson, James E.
supporting information; experimental part, p. 136 - 139 (2010/03/25)
"Chemical Equation Presented" A reaction sequence involving the chemoselective olefinic oxidation of W(1)-benzyl-2,7-dihydro-1H-azepine with m-CPBA in the presence of HBF4 and BnOH followed by ring contraction facilitates the stereoselective pr
Stereospecific Photochemical Cyclization of Azidoquinone with E,E- and Z,Z-Dienes. Application to the Synthesis of an Importent Precursor toward Mitomycins
Naruta, Yoshinori,Nagai, Naoshi,Yokota, Tadafumi,Maruyama, Kazuhiro
, p. 1185 - 1188 (2007/10/02)
Photochemical reaction of 5-azido-2-methoxy-3-methyl-1,4-benzoquinone with cis,cis-2,4-hexadien-1,6-diol derivatives stereoselectively affords the corresponding 2,3-dihydroindolquinone, which possesses trans configuration at 2,3-position and vinylic double bond preserves the original stereochemistry of the diene.It is efficiently converted to a key precursor in mitomycin synthesis.
