117701-67-4 Usage
Uses
Used in Organic Synthesis:
2-Furanol,3,3-dichlorotetrahydro-(9CI) is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
2-Furanol,3,3-dichlorotetrahydro-(9CI) is used as a research compound in the development of new drugs. Its chemical properties and reactivity with other substances can be exploited to design and synthesize novel pharmaceutical agents with potential therapeutic applications.
Used in Chemical Compatibility Studies:
2-Furanol,3,3-dichlorotetrahydro-(9CI) is used in studies to evaluate its compatibility with other chemical substances. Understanding its reactivity and interactions with other compounds can provide insights into its potential applications and limitations in various chemical processes and formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 117701-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,0 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117701-67:
(8*1)+(7*1)+(6*7)+(5*7)+(4*0)+(3*1)+(2*6)+(1*7)=114
114 % 10 = 4
So 117701-67-4 is a valid CAS Registry Number.
117701-67-4Relevant academic research and scientific papers
ω-SUBSTITUTED α,α-DICHLOROALDEHYDES AND DERIVATIVES VIA FORMOLYSIS OR ACETOLYSIS OF 2,3,3-TRICHLOROTETRAHYDROFURAN AND 2,3,3-TRICHLOROTETRAHYDROPYRAN
Buyck, Laurent de,Vanhulle, Peter
, p. 329 - 336 (2007/10/02)
Preferable routes to the 2-hydroxyderivatives 7 resp. 8 of 2,3,3-trichloroTHF (1) or 2,3,3-trichloroTHP (2) involve the uncatalyzed methanolysis of the corresponding 2-formates or 2-acetates.These activated esters were rapidly formed from 1 or 2 in a hot
2,2,4-TRICHLOROBUTANAL: AN INVITATION TO THE SYNTHESIS OF HETEROCYCLIC COMPOUNDS
Buyck, L. De,Menke, N.,Schamp, N.
, p. 121 - 126 (2007/10/02)
The title aldehyde (1) was obtained in 69percent isolated yield by chlorination of 4-chlorobutanol in the presence of dimethylformamide. 3,3-Dichloro-2-hydroxytetrahydrofuran (3a) or the 2-alkoxyderivatives 3b and 3c were produced by treating the hydrate 2a or the hemiacetals 2b and 2c resp. with base.With aqueous ammonia 1 rapidly formed the hemiaminal which then slowly afforded 3,3-dichloro-1-pyrroline (4).In a rapid reaction with primary alkylamines 1 was converted to N-alkyl-3,3-dichloro-2-hydroxypyrrolidines (5).The 2-hydroxyl group in 5 was reversibly exchanged in the presence of alcohols or amines. 5 were converted to N-alkyl-3,3-dichloro-1-pyrrolinium salts by an excess of trifluoroacetic acid.
