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54769-01-6

Trithiocarbonic acid 4-methoxy-benzyl ester methyl ester is a complex organic compound with the chemical formula C10H12O3S3. It is a derivative of trithiocarbonic acid, featuring a 4-methoxy-benzyl group and a methyl ester group attached to the central sulfur atom. Trithiocarbonic acid 4-methoxy-benzyl ester methyl ester is characterized by its unique structure, which includes three sulfur atoms bonded to a central carbon atom, with the 4-methoxy-benzyl and methyl ester groups providing additional functional groups. It is synthesized through a series of chemical reactions and is used in various applications, such as in the production of pharmaceuticals and as a chemical intermediate in the synthesis of other organic compounds. The compound's properties, such as its reactivity and stability, are influenced by the presence of the methoxy and ester groups, making it a versatile molecule in organic chemistry.

54769-01-6

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54769-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54769-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54769-01:
(7*5)+(6*4)+(5*7)+(4*6)+(3*9)+(2*0)+(1*1)=146
146 % 10 = 6
So 54769-01-6 is a valid CAS Registry Number.

54769-01-6Downstream Products

54769-01-6Relevant articles and documents

FERROCENYLTRITHIOCARBONATES I. DIRECT ACCESS FROM α-FERROCENYLCARBINOLS BY A SNi MECHANISM. ABSOLUTE X-RAY STRUCTURE DETERMINATION OF (R)-FERROCENYLMETHYLMETHANE S-METHYLTRITHIOCARBONATE

Patin, Henri,Mignani, Gerard,Mahe, Christian,Marouille, Jean-Yves Le,Benoit, Alain,Grandjean, Daniel

, p. 93 - 104 (2007/10/02)

Ferrocenyltrithiocarbonates (I) are readily obtained by treating α-ferrocenylcarbinols (II) successively with sodium hydride, carbon disulfide and alkyl halide.Formation of I occurs by intramolecular nucleophilic displacement of oxygen by sulfur with retention of configuration.This is supported by the nature of the other products formed and by the X-ray structure determination of an optically active compound I, which was refined to R = 0.038.The title compound of R configuration was obtained from (R)-ferrocenylmethylmethanol.

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