4- Chlorobenzyl chloride

Chlorobenzyl chloride Ambenonium chloride Ticlopidine HCI p-Chlorobenzyl chloride Clobutinol Echonazole nitrate Indomethacin Pyrrobutamine Triparanol 

Chlorobenzyl chloride 1950 2-Chloro-/>-phenylenediamine 1876 Citronellol acetate 4199 

Chlorobenzyl chloride (l-Chloro-2-(chloromethyl)benzene) (Chlorobromomethane) see Bromochloromethane (2-Chloro-1,3-butadiene) see Chloroprene (1-Chlorobutane) see n-Butylchloride (l-Chloro-2-(chloromethyl)benzene) see 2-Chlorobenzyl chloride 611-19-8 C Sensitizatii 

Diethyl Amino Ethyl Amine Ethyl Oxalate 2-Chlorobenzyl Chloride 

In one route, ticlopidine (1) was assembled via Sn2 displacement of 2-chlorobenzyl chloride (9) with 4,5,6,7-tetrahydro-thieno[3,2-c]pyridine (8).10,11 The 

The chlorination of benzyl chloride over H-K-L, K-L, K-beta, K-mordenite, K-ZSM-5, K-Y, and K-X, and in the absence of catalyst, at 353 K produces a mixture of 2-chlorobenzyl chloride (2-CIBC), 3-chlorobenzyl chloride (3-CIBC), 

One representative synthesis of prothioconazole starts [95] with the addition of the Grignard derivative of 2-chlorobenzyl chloride on the carbonyl double bond of chloromethyl 1-chloro-cyclopropyl ketone (Scheme 17.19). The untouched chlorine atom of the chloromethyl group is then classically substituted with 1,2,4-triazole. From this intermediate, one way to obtain the 2,4-dihydro-3H-l,2,4-triazole-3-thione of prothioconazole is by direct lithiation of the 1,2,4-triazole at position 5 with n-butyl lithium and reaction with sulfur. The commercially available compound is a mixture of two enantiomers (chirality of the quaternary carbon bearing the hydroxy group). 

Beilstein Handbook Reference) AI3-14885 Benzene, 1-chloro-2-(chloromethyl)- BRN 0471700 1-Chloro-2-(chloromethyl)benzene 2-Chlorobenzyl chloride a,2-Dichlorotoluene a,o-Dichlorotoluene EINECS 210-258-8 NSC 8446 o-Chlorobenzyl chloride Ortho-a-dichlorotoluene Toluene, a,o-dichloro- Toluene, o,a-dichloro-. Liquid mp = -17° bp = 217° d° = 1.2699 Am = 271, 278 nm (s = 339, 263, MeOH) insoluble in H2O, slightly soluble in EtOH, CCU, soluble in CS2, very soluble in Et20, CeHe, AcOH, 

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