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2-(4-Bromo-benzylsulfanylmethyl)-pyridine is a complex organic chemical compound characterized by a pyridine ring, which is a six-membered aromatic ring containing two nitrogen atoms. 2-(4-Bromo-benzylsulfanylmethyl)-pyridine features a 4-bromo-benzylsulfanylmethyl group attached to the 2-position of the pyridine ring. The 4-bromo-benzylsulfanylmethyl group consists of a benzyl group (a phenyl ring with a methyl group attached), a sulfur atom, and a bromine atom at the 4-position of the benzyl group. The presence of the bromine atom and the sulfur atom in the molecule may contribute to its reactivity and potential applications in various chemical processes, such as in the synthesis of pharmaceuticals or other specialty chemicals. The compound's unique structure and functional groups make it a potentially valuable intermediate in organic synthesis.

83782-63-2

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83782-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83782-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83782-63:
(7*8)+(6*3)+(5*7)+(4*8)+(3*2)+(2*6)+(1*3)=162
162 % 10 = 2
So 83782-63-2 is a valid CAS Registry Number.

83782-63-2Downstream Products

83782-63-2Relevant academic research and scientific papers

2-pyridine Derivatives: New Antiinflammatory Agents

Haviv, Fortuna,DeNet, Robert W.,Michaels, Raymond J.,Ratajczyk, James D.,Carter, George W.,Young, Patrick R.

, p. 218 - 222 (2007/10/02)

2-pyridine derivatives (1a-e) inhibited the dermal reverse passive Arthus reaction (RPAR) in the rat.In the same model, indomethacin was inactive, and hydrocortisone was active.Compounds 1a-d also significantly reduced exudate volume and white blood cell accumulation in the pleural RPAR.This pattern of activity was similar to that of hydrocortisone and different from that of indomethacin.

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