HRID339427

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCc1nn(C)c(C(=O)NCc2ccc(C(C)(C)C)cc2)c1Cl

HCID86354

Tebufenpyrad

C18H24ClN3O

HCID86356

Fenazaquin

C20H22N2O

结构：CC(C)(C)c1ccc(CSc2cnn(C(C)(C)C)c(=O)c2Cl)cc1

HCID91754

Pyridaben

C19H25ClN2OS

$结构：Cc1nn(C)c(Oc2ccccc2)c1/C=N\OCc1ccc(C(=O)OC(C)(C)C)cc1$

HCID6002001

(Z)-Fenpyroximate

C24H27N3O4

结构：CCOCCc1ccc(OCCNc2ncnc(CC)c2Cl)c(C)c1C

HCID6451139

Pyrimidifen

C20H28ClN3O2

结构：CCc1nn(C)c(C(=O)NCc2ccc(Oc3ccc(C)cc3)cc2)c1Cl

HCID10110536

Tolfenpyrad

C21H22ClN3O2

PRODUCTS

生成物

结构：Cc1ccc(/N=C/N(C)/C=N/c2ccc(C)cc2C)c(C)c1

HCID178426515

未命名化合物

PROCEDURE

实验过程

METI acaricides and insecticides: fenazaquin, fenpyroximate, pyridaben, pyrimidifen, tebufenpyrad, tolfenpyrad

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d1a08e4562eb4f478842d6c852ae864e
来源数据集: uspto-grants-2014_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08895035B2
来源说明: uspto-grants-2014_11

反应 SMILES

CC(C1C=CC(CCO[C:14]2[N:23]=[CH:22][N:21]=C3C=2C=CC=C3)=CC=1)(C)C.CC1C(/C=N\OC[C:34]2[CH:39]=[CH:38][C:37]([C:40](OC(C)(C)C)=O)=[CH:36][CH:35]=2)=C(OC2C=CC=CC=2)N(C)N=1.CC(C1C=CC(CSC2C=N[N:71](C(C)(C)C)[C:69](=O)C=2Cl)=CC=1)(C)C.CCC1N=CN=C(NCCO[C:91]2[CH:96]=[CH:95][C:94]([CH2:97]COCC)=[C:93](C)[C:92]=2[CH3:103])C=1Cl.[CH3:105]CC1C(Cl)=C(C(NCC2C=CC(C(C)(C)C)=CC=2)=O)N(C)N=1.CCC1C(Cl)=C(C(NCC2C=CC(OC3C=CC(C)=CC=3)=CC=2)=O)N(C)N=1>>[CH3:97][C:94]1[CH:95]=[CH:96][C:91](/[N:21]=[CH:22]/[N:23]([CH3:14])/[CH:69]=[N:71]/[C:34]2[CH:35]=[CH:36][C:37]([CH3:40])=[CH:38][C:39]=2[CH3:105])=[C:92]([CH3:103])[CH:93]=1