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α-trichloromethyl-(3-nitrophenyl)carbinol is a complex organic compound characterized by its chemical structure, which includes a trichloromethyl group (CCl3), a 3-nitrophenyl group (C6H4NO2), and a hydroxyl group (-OH). This molecule is known for its unique properties, which arise from the combination of a highly reactive trichloromethyl moiety and a nitrophenyl ring. The trichloromethyl group is electron-withdrawing and can participate in various chemical reactions, while the nitro group on the phenyl ring introduces additional reactivity and can influence the compound's stability and physical properties. The hydroxyl group further adds to the molecule's reactivity, making it a potential precursor in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure and reactivity, α-trichloromethyl-(3-nitrophenyl)carbinol is of interest in organic chemistry research and development.

54619-63-5

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54619-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54619-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,1 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54619-63:
(7*5)+(6*4)+(5*6)+(4*1)+(3*9)+(2*6)+(1*3)=135
135 % 10 = 5
So 54619-63-5 is a valid CAS Registry Number.

54619-63-5Relevant academic research and scientific papers

CHARACTERIZATION OF THE ACTUAL CATALYTIC AGENT IN POTASSIUM FLUORIDE ON ACTIVATED ALUMINA SYSTEMS

Weinstock, Leonard M.,Stevenson, James M.,Tomellini, Sterling A.,Pan, Shih-Hsie,Utne, Torleif,et al.

, p. 3845 - 3848 (1986)

The spectral and chemical properties of potassium fluoride on activated alumina, an extensively used basic catalyst in organic synthesis, show that its unusually high reactivity relative to other fluoride-containing basic systems is due to the reaction of

A method for preparing chlorine Shu Long

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Paragraph 0026-0028, (2017/02/17)

The invention discloses a preparation method of clorsulon. The preparation method comprises the steps: carrying out condensation on m-nitrobenzaldehyde with chloroform at a low temperature, then chloridizing, and carrying out elimination, hydrazine hydrate reduction, chlorosulfuric acid sulphonation and ammonification to obtain clorsulon. The use of benzene with relatively high toxicity is avoided, the use of chlorine with relatively large dangerousness is also avoided, the reduction reaction adopts more environmentally-friendly hydrazine hydrate, hydrazine hydrate reduction has less solid waste than iron powder reduction, an excellent catalyst ferric trichloride and an activated carbon carrier are selected, a by-product nitrogen gas has a good protective effect on the product, the product quality is high, the yield is equivalent to the yield reported in literature, the process is simplified, reaction conditions are mild, and the preparation method is environmentally friendly and has good industrial application prospects.

Decarboxylative trichloromethylation of aromatic aldehydes and its applications in continuous flow

Jensen, Andreas B.,Lindhardt, Anders T.

, p. 1174 - 1183 (2014/03/21)

Two new protocols for the efficient synthesis of 2,2,2- trichloromethylcarbinols, starting from aromatic aldehydes, have been developed. A combination of sodium trichloroacetate in the presence of malonic acid proved efficient for the transformation of el

COMPOUNDS AND THEIR SALTS SPECIFIC TO THE PPAR RECEPTORS AND THE EGF RECEPTORS AND THEIR USE IN THE MEDICAL FIELD

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Paragraph 0054; 0055, (2013/05/22)

The present invention relates to compounds comprising the general formula (I), in which R1 and R2, which may be identical or different, are selected from the group comprising —H or a linear or branched alkyl group having from 1 to 6 carbon atoms or togeth

Compounds and Their Salts Specific to the PPAR Receptors and the EGF Receptors and Their Use in the Medical Field

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Page/Page column 7-8, (2009/03/07)

The present invention relates to compounds comprising the general formula (I), in which R1 and R2, which may be identical or different, are selected from the group comprising —H or a linear or branched alkyl group having from 1 to 6

FLUORIDE-ALUMINA REAGENTS: THE ACTIVE BASIC SPECIES

Ando, Takashi,Clark, James H.,Cork, David G.,Hanafusa, Terukiyo,Ichihara, Junko,Kimura, Takahide

, p. 1421 - 1424 (2007/10/02)

Comparison of KF and NaF impregnated on active alumina shows that the formation of strong base by fluoride reaction with alumina cannot totally explain the extremely high reactivity of KF-alumina as a heterogeneous base for catalytic as well as non catalytic reactions.At least three mechanisms apparently give rise to the high basicity.

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