103364-68-7 Usage
Description
(1S,2S)-cyclohexa-3,5-diene-1,2-diol is a chemical compound with the molecular formula C6H8O2. It is a diol, meaning it contains two hydroxyl (-OH) groups. (1S,2S)-cyclohexa-3,5-diene-1,2-diol is a stereochemically defined form of cyclohexa-1,2-diol, which is a cyclic diol with a six-membered ring structure. The (1S,2S) stereochemistry indicates the specific arrangement of atoms around the stereocenter at positions 1 and 2 in the cyclohexane ring. This unique stereochemistry can have implications for its reactivity and interactions with other molecules in chemical reactions.
Uses
Used in Organic Synthesis:
(1S,2S)-cyclohexa-3,5-diene-1,2-diol is used as a building block in organic synthesis for its unique stereochemistry and reactivity. Its specific arrangement of atoms allows for the creation of complex molecules with desired properties, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1S,2S)-cyclohexa-3,5-diene-1,2-diol is used as a key intermediate in the synthesis of various drug molecules. Its stereochemistry plays a crucial role in determining the biological activity and selectivity of the final drug product, contributing to the development of more effective and targeted therapies.
Used in Agrochemical Industry:
(1S,2S)-cyclohexa-3,5-diene-1,2-diol is also utilized in the agrochemical industry as a precursor for the synthesis of pesticides and other crop protection agents. Its unique properties enable the development of more effective and environmentally friendly solutions for agricultural applications.
Used in Specialty Chemicals:
In the specialty chemicals sector, (1S,2S)-cyclohexa-3,5-diene-1,2-diol is employed as a versatile building block for the synthesis of various high-value compounds. Its stereochemistry and reactivity make it suitable for the production of advanced materials, fragrances, and other specialty products.
Check Digit Verification of cas no
The CAS Registry Mumber 103364-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,6 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103364-68:
(8*1)+(7*0)+(6*3)+(5*3)+(4*6)+(3*4)+(2*6)+(1*8)=97
97 % 10 = 7
So 103364-68-7 is a valid CAS Registry Number.
103364-68-7Relevant articles and documents
Highly enantio- and diastereo-selective synthesis of C2-symmetric 3,5-cyclohexadiene-1,2-diol and D2-symmetric cyclohexane-1,2,4,5-tetrol
Suemune,Hasegawa,Sakai
, p. 55 - 58 (2007/10/02)
Highly enantio- and diastereo-selective synthesis of C2-symmetric 3,5-cyclohexadiene-1,2-diol 5 and D2-symmetric cyclohexane-1,2,4,5-tetrol related compounds 7a,b 10, 11 has been achieved using optically active 4-cyclohexene-1,2-diol
Resolution of trans-1,2-Dihydroxy-1,2-dihydrobenzene for the Preparation of Optically Pure Benzene Diol Epoxides. Preparation of Bromo- and Chlorobenzene Diol Epoxides
Ganey, Michael V.,Padykula, Robert E.,Berchtold, Glenn A.,Braun, Andrew G.
, p. 2787 - 2793 (2007/10/02)
The resolution of (+/-)-trans-1,2-dihydroxy-1,2-dihydrobenzene has been accomplished by esterase-catalysed hydrolysis of diacetate (+/-)-5.Peracid epoxidation of (+)-2 and (-)-2 gave diol epoxides (+)-3 and (-)-3, respectively.The synthesis of d
