70415-58-6 Usage
Uses
Used in Polymer Synthesis:
(Z)-1,3-Butadien-1-ol is used as a monomer in the polymer industry for the production of various synthetic rubbers and plastics. Its reactivity and versatility in chemical reactions make it a valuable component in the synthesis of a wide range of polymeric materials.
Used in Fragrance Production:
Isoprene alcohol is utilized as a key ingredient in the fragrance industry, where it contributes to the creation of diverse scents and perfumes. Its sweet odor and ability to blend well with other compounds make it a sought-after component in the formulation of fragrances.
Used as a Chemical Intermediate:
(Z)-1,3-Butadien-1-ol also serves as a chemical intermediate in the synthesis of other organic compounds. Its unique structure allows it to be a building block for a variety of chemical products, further expanding its applications across different industries.
Safety Precautions:
Given its highly flammable and reactive properties, (Z)-1,3-Butadien-1-ol requires special attention during handling and storage. Proper safety measures, including the use of protective equipment and adherence to safety protocols, are essential to minimize risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 70415-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,1 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70415-58:
(7*7)+(6*0)+(5*4)+(4*1)+(3*5)+(2*5)+(1*8)=106
106 % 10 = 6
So 70415-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O/c1-2-3-4-5/h2-5H,1H2/b4-3-
70415-58-6Relevant academic research and scientific papers
Capon, Brian,Guo, Bozhang
, p. 5144 - 5147 (1988)
(Z)- and (E)-1-hydroxybutadiene have been generated from their trimethylsilyl derivatives in slightly acidic aqueous acetonitrile and CH3OH-DMSO mixtures and characterized by NMR spectroscopy.The kinetics and products of ketonization of both dienols have been investigated.In aqueous solution they yield mixtures of (E)-2-butenal and 3-butenal whose proportions depend on pH.Analysis of the variation of product composition with pH indicates that (E)-1-hydroxybutadiene yields 90.1, 28.0, and 44.7percent of (E)-2-butenal in the H3O+, H2O, and HO--catalyzed reactions, whereas (Z)-1-hydroxybutadiene yields 69.8, 17.2, and 19.6percent.It is suggested that transmission of positive charge to the oxygen in the transition state for protonation at the 4-position is more efficient with the E than with the Z isomer, possibly because it is easier for the former to attain a planar conformation.No evidence was found for a mechanism that involves a cyclic transition state for the spontaneous ketonization of (Z)-butadienol.
