Detail of "84824-76-0"

Reference

2-Cyanoethyl imidazoledithiocarboxylates

2-Cyanoethyl imidazoledithiocarboxylates. (Shikoku Chemicals Corp., Japan). Jpn. Kokai Tokkyo Koho JP 59184164 A2 19 Oct 1984 Showa, 7 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: IC: C07D233-64. APPLICATION: JP 83-57132 31 Mar 1983. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The title compds. I (R = Me, H, Et, undecyl, heptadecyl, Ph; R1 = H, Me; R2 = CH2CH2CN) were prepd. by addn. reaction of I (R2 = H) with NCCH:CH2. Thus, heating a mixt. There are some commonly used reagents like 84824-76-0 in this article. of 4.3 g I (R-R2 = H), 15 mL DMF, and 3.2 g NCCH:CH2 at 70-80° for 3 h gave 0.8 g I (R = R1 = H, R2 = CH2CH2CN). .

Imidazoledithiocarboxylic acid esters

Imidazoledithiocarboxylic acid esters. (Shikoku Chemicals Corp., Japan). Jpn. Kokai Tokkyo Koho JP 60019769 A2 31 Jan 1985 Showa, 12 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM: C07D233-90. APPLICATION: JP 83-128473 13 Jul 1983. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Title compds. I (R = H, Me; R1 = H, Me, Et, undecyl, heptadecyl, Ph; R2 = Me, Et, Pr, Bu, lauryl, PhCH2) were prepd. Thus, stirring I (R-R3 = H) with EtI and Ca(OH)2 in H2O at 60-70° for 2 h gave 73. 84824-76-0 is just another one chemical used in this study.6% I (R = R1 = H, R2 = Et). .