99566-50-4 Usage
Uses
Used in Organic Synthesis:
(2R,3E)-3-methyl-4-(3-phenoxyphenyl)but-3-ene-1,2-diol is used as a building block in organic synthesis for the creation of more complex molecules and compounds. Its unique structure and functional groups make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
(2R,3E)-3-methyl-4-(3-phenoxyphenyl)but-3-ene-1,2-diol is used as a starting material for the preparation of pharmaceutical compounds. Its specific properties and reactivity can be utilized to develop new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
(2R,3E)-3-methyl-4-(3-phenoxyphenyl)but-3-ene-1,2-diol is used as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its unique structure and functional groups can contribute to the development of more effective and environmentally friendly products.
Used in Specialty Chemicals:
(2R,3E)-3-methyl-4-(3-phenoxyphenyl)but-3-ene-1,2-diol is used as a starting material for the preparation of specialty chemicals, such as fragrances, dyes, and other industrial chemicals. Its versatility and reactivity make it a valuable component in the development of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 99566-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,6 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 99566-50:
(7*9)+(6*9)+(5*5)+(4*6)+(3*6)+(2*5)+(1*0)=194
194 % 10 = 4
So 99566-50-4 is a valid CAS Registry Number.
99566-50-4Relevant academic research and scientific papers
Absolute Structure and Activity Relationships of Cinnamyl Alcohol Derivatives of Pyrethroid Insecticides
Matsuo, Noritada,Yano, Toshihiko,Ohno, Nobuo
, p. 3029 - 3036 (2007/10/02)
Synthesis of three optically active pyrethroids containing cinnamyl-type alcohol moieties, and their insecticidal activity are reported.The presence of a m-phenoxy group at a benzene ring inverted the structure-activity relationships dramatically with respect to the absolute configuration of alcohol moieties.
