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4-benzyl-2,3,6-trichloro-5-(2-tetrahydrofuryl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74894-27-2

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74894-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74894-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,9 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74894-27:
(7*7)+(6*4)+(5*8)+(4*9)+(3*4)+(2*2)+(1*7)=172
172 % 10 = 2
So 74894-27-2 is a valid CAS Registry Number.

74894-27-2Downstream Products

74894-27-2Relevant academic research and scientific papers

Polyhalogenoaromatic Compounds. Part 42. 13C N.m.r. Spectra of Polyhalogeno-pyridines and pyrimidines

Iddon, Brian,Mack, Arthur G.,Suschitzky, Hans,Taylor, Jack A.,Wakefield, Basil J.

, p. 1370 - 1380 (2007/10/02)

13C N.m.r. spectra are reported for a number of polyhaloheno-pyridines and -pyrimidines.Substituent effects have been calculated and the results used to assign structures.

Polyhalogenoaromatic Compounds. Part 41. Photochemical Dehalogenation and Arylation Reactions of Polyhalogenoaromatic and Polyhalogenoheteroaromatic Compounds

Bratt, Jack,Iddon, Brian,Mack, Arthur G.,Suschitzky, Hans,Taylor, Jack A.,Wakefield, Basil J.

, p. 648 - 656 (2007/10/02)

Photolysis of pentachloro- and pentabromo-pyridine in diethyl ether or methanol leads to loss of β-halogen.A product (9) derived from attack on diethyl ether was also identified. 4-Bromotetrachloropyridine also undergoes loss of bromine and tetrachloro-4-iodopyridine loses iodine exclusively.Photodehalogenation of some perhalogenothiophens, tetrachloropyrimidine, and hexachlorobenzene is also described.Photolysis of pentachloroiodobenzene, tetrachloroiodopyridines, and trichloro-5-iodothiophen in benzene gives the corresponding polychloroaryl- or polychloroheteroaryl-benzenes.Photolysis of tetrachloro-4-(phenylthio)pyridine (3) gives 1,3,4-trichlorobenzothienopyridine (6), and the analogous perchloro(phenylthio)pyridine (37) gives the corresponding perchlorobenzothienopyridine (61).The scope of this type of photocyclisation has been explored; starting materials investigated include various arylthiopolyhalogenopyridines, some arylamino- and aryloxy-tetrachloropyridines, and 4-anilinotrichloropyrimidine.

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