75089-05-3 Usage
Type of compound
Unsaturated alcohol
Structural features
Contains a carbon-carbon triple bond and a double bond in the Z configuration
Common uses
Synthesis of various organic molecules
Precursor for
Production of other alcohols, ketones, and aldehydes
Potential applications
Pharmaceutical and agrochemical industries
Unique structure
Valuable building block for a wide range of organic compounds
Reactivity
Due to its unsaturated nature and functional groups, it can undergo various chemical reactions such as hydrogenation, oxidation, and addition reactions
Solubility
Generally soluble in organic solvents like ethanol, methanol, and acetone
Stability
Stable under normal conditions, but sensitive to heat, light, and strong acids or bases
Purity
Typically synthesized with high purity for use in chemical reactions and applications
Safety precautions
Handle with care, as it may be flammable or toxic depending on its concentration and exposure
Storage
Store in a cool, dry, and well-ventilated area, away from heat and direct sunlight
Regulatory status
May be subject to specific regulations depending on its intended use and concentration in a product
Environmental impact
Potentially biodegradable, but its environmental impact depends on its concentration, use, and disposal methods.
Check Digit Verification of cas no
The CAS Registry Mumber 75089-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,8 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75089-05:
(7*7)+(6*5)+(5*0)+(4*8)+(3*9)+(2*0)+(1*5)=143
143 % 10 = 3
So 75089-05-3 is a valid CAS Registry Number.
75089-05-3Relevant academic research and scientific papers
A STEREOSELECTIVE SYNTHESIS OF (Z)-13-HEXADECEN-11-YNYL ACETATE, THE SEX PHEROMONE OF Thaumetopoea pityocampa (LEPIDOPTERA, NOTODONTIDAE)
Cardillo, Giuliana,Cugola, Alfredo,Orena, Mario,Sandri, Sergio
, p. 231 - 234 (2007/10/02)
(Z)-13-Hexadecen-11-ynyl acetate, 1, the sex pheromone of Thaumetopoea pityocampa, has been synthesized stereospecifically, starting from anion of 3--1-hexyne, 8, which was alkylated with 10-iodo-1-decane; the intermediate diol 2, obtained upon removal of the protecting groups was stereoselectively dehydrated with KHSO4.
