3893-10-5 Usage
Uses
Used in Organic Synthesis:
1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is used as a building block for the synthesis of various compounds, contributing to the development of a wide range of chemical products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is used as a key intermediate for the production of different pharmaceuticals, playing a crucial role in the development of new medications.
Used in Agrochemical Synthesis:
1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is also utilized as an intermediate in the synthesis of agrochemicals, aiding in the creation of products for agricultural applications.
Used in Optical Material Development:
Within the optical materials industry, 1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is used as a component for developing materials that leverage its light absorption and fluorescence properties.
Used in Sensor Development:
1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is employed in the development of sensors, taking advantage of its light absorption and fluorescence characteristics to enhance sensor performance and sensitivity.
Used in Anticancer Research:
In the field of biological research, 1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is studied for its potential anticancer properties, with the aim of discovering new therapeutic approaches for cancer treatment.
Used in Antioxidant Research:
Similarly, 1-(4-METHOXYPHENYL)-6-PHENYLHEXATRIENE is investigated for its antioxidant properties, which may lead to applications in the development of products that combat oxidative stress and related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 3893-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,9 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3893-10:
(6*3)+(5*8)+(4*9)+(3*3)+(2*1)+(1*0)=105
105 % 10 = 5
So 3893-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H18O/c1-20-19-15-13-18(14-16-19)12-6-3-2-5-9-17-10-7-4-8-11-17/h2-16H,1H3/b3-2+,9-5+,12-6+
3893-10-5Relevant academic research and scientific papers
Stereoselective approaches to (E,E,E) and (Z,E,E)-α-chloro-ω- substituted hexatrienes: Synthesis of all E polyenes
Crousse, Benoit,Mladenova, Margarita,Ducept, Pascal,Alami, Mouad,Linstrumelle, Gerard
, p. 4353 - 4368 (2007/10/03)
Two stereocontrolled synthetic approaches to (E,E,E) and (Z,E,E)-α- chloro-ω-substituted hexatrienes 1-3 are described starting from unsaturated compounds 4-6. The key step of the first approach is based on the palladium- catalyzed rearrangement of bis-allylic acetates 4 and 5 and the second one is based on the stereoselective reduction of homopropargylic alcohols 6 followed by an elimination reaction. These stable chlorotrienes 1-3 are suitable synthetic intermediates for the construction of navenone B and all E polyenes (trienes, tetraenes, hexaenes and heptaenes).
Stereocontrolled synthesis of (E,E,E)-chlorotrienes: Efficient intermediates for the construction of all E conjugated polyenes
Crousse, Benoit,Alami, Mouad,Linstrumelle, Gerard
, p. 5297 - 5300 (2007/10/03)
Stereoselective reduction of conjugated homopropargylic alcohols 1 followed by an elimination reaction, allows an efficient approach to stereodefined (E,E,E)-chlorotrienes. The interest of these chlorotrienes was illustrated by a stereocontrolled synthesis of navenone B and all E conjugated polyenes (trienes, tetraenes and hexaenes).
