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4-Chloro-1,3-benzenediol

Beilstein Handbook Reference) AI3-03873 1,3-Benzenediol, 4-chloro- BRN 2042864 4-Chloro-1,3-benzenediol 4-Chloro-1,3Klihydroxy-benzene 4-Chlororesorcin 4-Chlororesorcinol 6-Chlororesorcinol p-Chlorotesorcinol Cl 76510 2,4-... [Pg.137]

CAS 95-88-5 EINECS/ELINCS 202-462-0 Synonyms 1,3-Benzenediol, 4-chlor- 4-Chloro-1,3-benzenediol Cl 76510... [Pg.913]

Chloro-1,3-benzenediol 2-Chloro-1,4-benzenediol 2-Chlorobenzenemetlianamine 3-Chlorobenzenemethanamine... [Pg.227]

Chloro-1,3-dinitro-5-trilluoromethylbenzene, 2637 Dimethyl 4-acetamidophthalate Nitric acid, 3520 4,6-Dinitro-l,3-benzenediol, 2198 Dinitrogen tetraoxide, Laboratory grease, 4747... [Pg.266]

Figure 19.2. Prediction of the contact allergenicity of 4-chloro-l,3-benzenediol. In addition to the probability of activity and the basal potency derived from the toxicophore (shown in bold in A), the chemical also contains an activating modulator (shown in bold in B), which further augments the potency. A potency of 64 units indicates a very strong potency (Table 19.3). Figure 19.2. Prediction of the contact allergenicity of 4-chloro-l,3-benzenediol. In addition to the probability of activity and the basal potency derived from the toxicophore (shown in bold in A), the chemical also contains an activating modulator (shown in bold in B), which further augments the potency. A potency of 64 units indicates a very strong potency (Table 19.3).
C6H5CI02 3-chloro 1,2-benzenediol 4018-65-9 25.00 1.2934 2 6909 C6H6BrN 2-bromo-5-methyl pyridine 3510-66-5 35.83 1.5426 2... [Pg.221]

C6H5CI02 4-chloro-1,2-benzenediol 2138-22-9 25.00 1.2934 2 6917 C6H6Br2N2 2-bromo-2-(bromomethyl)pentanedinitrile 35691-65-7 25.00 1.9549 2... [Pg.221]

C6H5CI02 5-chloro-1,3-benzenediol 52780-23-1 25.00 1.2934 2 6920 C6H6CIFN2 4-chloro-5-fluoro-o-phenylenediamine 132942-81-5 25.00 1.3011 2... [Pg.221]

C10H14CIN 4-chloro-N,N-diethylaniline 2873-89-4 25.00 1.0345 2 20099 C10H14O2 2-methyl-5-isopropyl-1,4-benzenediol 2217-60-9 21.73 1.0338 2... [Pg.253]

Dihydroxy-9(10i/)-anthracenone 380—see also AnthraUn, Dithranol Dihydroxyanthraquinones, chemical shifts for, isotope effects on 345, 346 Dihydroxybenzenes—see also Benzenediols, 4-Chloro-l, 2/3-dihydroxybenzenes, Dihydroxyalkylbenzenes, Hydroxyphenols methylation of 308 synthesis of 408, 409, 411... [Pg.1486]

Chlorobenzenecarboperoxoicacid 4-Chloro-1.2-benzenediamine 4-Chloro-1.3-benzenediamine 2-Chloro-1,4-benzenediamine 3-Chloro-1,2-benzenediol 4-Chloro-1.2-benzenediol... [Pg.217]

Preparation by reaction of benzoyl chloride with 4-chloro-l,2-benzenediol in the presence of aluminium chloride at 140° for 4.5 h [1205]. [Pg.369]

See other pages where 4-Chloro-1,3-benzenediol is mentioned: [Pg.217]    [Pg.209]    [Pg.881]    [Pg.195]    [Pg.196]    [Pg.241]    [Pg.242]    [Pg.229]    [Pg.230]    [Pg.240]    [Pg.241]    [Pg.209]    [Pg.1284]    [Pg.1353]    [Pg.179]    [Pg.335]    [Pg.221]    [Pg.436]    [Pg.436]    [Pg.436]    [Pg.436]    [Pg.520]    [Pg.245]    [Pg.217]    [Pg.217]    [Pg.209]    [Pg.209]    [Pg.209]    [Pg.881]    [Pg.62]    [Pg.63]    [Pg.429]    [Pg.429]    [Pg.518]    [Pg.7170]    [Pg.195]    [Pg.195]    [Pg.195]    [Pg.195]    [Pg.196]    [Pg.196]    [Pg.241]    [Pg.241]    [Pg.241]    [Pg.241]    [Pg.242]    [Pg.242]    [Pg.227]    [Pg.227]   


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