51308-99-7 Usage
Uses
Used in Fragrance and Flavor Industry:
9-Chloro-1-nonanol is used as a raw material for the production of fragrances and flavors, leveraging its chemical properties to contribute to the development of scents and tastes in various consumer products.
Used in Chemical Synthesis:
9-Chloro-1-nonanol serves as a building block in the synthesis of other chemicals, playing a crucial role in the creation of a wide range of compounds for different applications.
Used in Surfactant and Emulsifier Production:
As a component in the production of surfactants and emulsifiers, 9-Chloro-1-nonanol is utilized for its ability to reduce the surface tension of liquids, facilitating the mixing of otherwise immiscible substances.
Used in Pharmaceutical Industry:
9-Chloro-1-nonanol has potential applications in the pharmaceutical sector, where its unique structure may contribute to the development of new drugs or drug formulations.
Used in Agrochemical Industry:
9-Chloro-1-nonanol also finds use in agrochemicals, potentially aiding in the development of pesticides, herbicides, or other agricultural chemicals to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 51308-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,0 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51308-99:
(7*5)+(6*1)+(5*3)+(4*0)+(3*8)+(2*9)+(1*9)=107
107 % 10 = 7
So 51308-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H19ClO/c10-8-6-4-2-1-3-5-7-9-11/h11H,1-9H2
51308-99-7Relevant academic research and scientific papers
Oxidation of monohydric and dihydric alcohols with CCl4 catalyzed by molybdenum compounds
Khusnutdinov,Shchadneva,Burangulova,Muslimov,Dzhemilev
, p. 1615 - 1621 (2007/10/03)
Mo(CO)6 catalyzed oxidation of alcohols and diols with tetrachloromethane. Primary oxidation products in reaction of alcohols with CCl4 are alkyl hypochlorites, and final products depending on the structure of initial alcohol are aldehydes (as acetals), ketones, chloroketones, and esters.
REGIOSPECIFIC AND STEREOSPECIFIC SUBSTITUTION OF HYDROXYL IN ALIPHATIC ALCOHOLS BY HALOGEN
Matveeva, E. D.,Kurts, A. L.,Yalovskaya, A. I.,Nikishova, N. G.,Bundel', Yu. G.
, p. 642 - 646 (2007/10/02)
A new system containing triphenylphosphine and trichloro- and tribromoacetic ester makes it possible to substitute the hydroxyl group in alcohols by halogen.Regiospecific and stereospecific substitution of the hydroxyl by the halogen takes place as a result of the reaction of primary and secondary aliphatic alcohols and of 2-alkenols, susceptible to isomerization processes, with this system.
