353-30-0 Usage
Uses
Used in Chemical Production:
1,12-Difluorododecane is used as an intermediate for the production of various chemicals and materials, including surfactants, lubricants, and polymers. Its unique properties make it a valuable component in the synthesis of these products.
Used in Solvent Applications:
Due to its solubility in organic solvents, 1,12-Difluorododecane is used as a solvent in various industrial processes. Its ability to dissolve a wide range of substances makes it a versatile option for different applications.
Used in Pharmaceutical Manufacturing:
1,12-Difluorododecane is used as a component in the manufacturing of pharmaceuticals. Its low toxicity and compatibility with other substances make it a suitable candidate for use in the development of new drugs and medications.
Used in Agrochemical Production:
In the agrochemical industry, 1,12-Difluorododecane is utilized in the production of various products, such as pesticides and fertilizers. Its properties contribute to the effectiveness and safety of these products when used in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 353-30-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 353-30:
(5*3)+(4*5)+(3*3)+(2*3)+(1*0)=50
50 % 10 = 0
So 353-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H24F2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-12H2
353-30-0Relevant articles and documents
Selective monofluorination of diols using DFMBA
Yoneda, Atsushi,Fukuhara, Tsuyoshi,Hara, Shoji
, p. 3589 - 3590 (2007/10/03)
Selective monofluorination of 1,2- and 1,3-diols was achieved by reaction with DFMBA. The method is applicable for the synthesis of optically-active fluorohydrin derivatives. The Royal Society of Chemistry 2005.
Deoxyfluorination of alcohols using N,N-diethyl-α,α-difluoro- (m-methylbenzyl)amine
Kobayashi, Shingo,Yoneda, Atushi,Fukuhara, Tsuyoshi,Hara, Shoji
, p. 6923 - 6930 (2007/10/03)
Deoxyfluorination of alcohols was carried out using N,N-diethyl-α, α-difluoro-(m-methylbenzyl)amine (DFMBA). Primary alcohols were effectively converted to fluorides under microwave irradiation or conventional heating. Deoxyfluorination of an anomeric hydroxy group in sugars by DFMBA proceeded at below room temperature and glycosyl fluorides could be obtained in good yields. The deoxyfluorination reaction chemoselectively proceeded and various protecting groups on the sugar can survive under the reaction conditions.
CHEMOSELECTIVE FLUORINATION FOR PRIMARY ALCOHOLS
Shimizu, Makoto,Nakahara, Yuko,Yoshioka, Hirosuke
, p. 4207 - 4210 (2007/10/02)
Primary alcohols and their silylated derivatives are selectively fluorinated by tetraalkylammonium fluoride and aryl (or alkyl) sulfonyl fluoride.
