217479-60-2 Usage
Description
2,4,6-Trichlorobenzyl Alcohol 97, also known as T774363, is an organic compound with the molecular formula C7H5Cl3O. It is a colorless to pale yellow liquid and is an intermediate in the synthesis of various chemicals. 2 4 6-TRICHLOROBENZYL ALCOHOL 97 is derived from 2,4,6-Trichlorobenzoic Acid (T774715), which is a possible degradation intermediate of Polychlorinated Biphenyls (PCBs) in contaminated soil, indicating the presence of microbial transformation processes over time.
Uses
Used in Chemical Synthesis:
2,4,6-Trichlorobenzyl Alcohol 97 is used as an intermediate in the synthesis of 1,3,5-Trichloro-2-methylbenzene (T774363) for various chemical applications.
Used in Hydrodechlorination Process:
1,3,5-Trichloro-2-methylbenzene, synthesized from 2,4,6-Trichlorobenzyl Alcohol 97, can be used as a reactant or reagent in the hydrodechlorination process, which is a method for removing chlorine atoms from organic compounds.
Used in Catalysts Production:
2,4,6-Trichlorobenzyl Alcohol 97 is also used in the production of catalysts for the conversion of polychlorotoluene-containing mixtures into 2,6-dichlorotoluene, which is an important industrial chemical.
Used in Environmental Remediation:
As a derivative of 2,4,6-Trichlorobenzoic Acid (T774715), 2,4,6-Trichlorobenzyl Alcohol 97 is involved in the microbial transformation processes that occur in contaminated soil, potentially playing a role in the degradation of harmful pollutants like PCBs.
Check Digit Verification of cas no
The CAS Registry Mumber 217479-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,4,7 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 217479-60:
(8*2)+(7*1)+(6*7)+(5*4)+(4*7)+(3*9)+(2*6)+(1*0)=152
152 % 10 = 2
So 217479-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl3O/c8-4-1-6(9)5(3-11)7(10)2-4/h1-2,11H,3H2
217479-60-2Relevant articles and documents
Direct Ruthenium-Catalyzed Hydrogenation of Carboxylic Acids to Alcohols
Cui, Xinjiang,Li, Yuehui,Topf, Christoph,Junge, Kathrin,Beller, Matthias
supporting information, p. 10596 - 10599 (2015/09/02)
The "green" reduction of carboxylic acids to alcohols is a challenging task in organic chemistry. Herein, we describe a general protocol for generation of alcohols by catalytic hydrogenation of carboxylic acids. Key to success is the use of a combination of Ru(acac)3, triphos and Lewis acids. The novel method showed broad substrate tolerance and a variety of aliphatic carboxylic acids including biomass-derived compounds can be smoothly reduced.
Sulfonamide compounds and medicinal use thereof
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Page column 126, (2010/02/04)
A sulfonamide compound of the formula (I):R 1 --SO 2 NHCO--A--R 2 (I)wherein R 1 is alkyl, alkenyl, alkynyl and the like; A is an optionally substituted heteropolycyclic group except benzimidazolyl, indolyl, 4,7-dihydrobenzimidazolyl and 2,3-dihydrobenzoxazinyl; X is alkylene, oxa, oxa(lower)alkylene and the like; and R 2 is optionally substituted aryl, substituted biphenylyl and the like, a salt thereof and a pharmaceutical composition comprising the same. The sulfonamide compound is effective for the diseases treatable based on their blood sugar level-depressing activity, cGMP-PDE (especially PDE-V)-inhibiting activity, smooth muscle relaxing activity, bronchodilating activity, vasodilating activity, smooth muscle cell suppressing activity, and antiallergic activity.
