部分構造検索

325141

CCCCCCCCC(C)(CCCCCCCC)CCCCCCCC
Reaction #2678
tri-n-octylmethylmethane
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC(Cl)(CCCCCCCCCC)CCCCCCCCCC
Reaction #2680
tri-n-decylmethylchloride
収率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC(C)(CCCCCCCCCC)CCCCCCCCCC
Reaction #2681
tri-n-decylmethylmethane
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCC(Cl)(CCCCCCCCCC)CCCCCCCCCC
Reaction #2685
di-n-decyl-n-tetradecyl-methylchloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCCC(Cl)(CCCCCCCCCC)CCCCCCCCCCCCCC
Reaction #2687
n-nonadecyl-n-tetradecyl-n-decylmethylchloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2cc(O)ccc21
Reaction #6602
title compound
収率 32.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(Cl)C(=O)CCCC1(Cl)Cl
Reaction #50115
2-allyl-2,3,3,trichlorocyclohexanone
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2c(O)cc(Br)cc21
Reaction #51271
3-bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCC/C(C)=C/CO.CC(C)=CCC/C(C)=C\CO
Reaction #55673
nerol geraniol
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74961
1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1=CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74963
6-tert-butyl-1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74964
1,2,3,4,9,9-hexachloro-1,4-dihydro-6-(phenylsulfonyl)-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(Cl)c(O)c2c1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74966
1,2,3,4,6,9,9-heptachloro-1,4-dihydro-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74968
crystals
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74969
1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(S(=O)(=O)c2ccccc2)C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74970
1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-6-phenylsulfonyl-1,4-methanonaphthalene-5,8-dione
収率 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCSC1CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74971
6-butylthio-1,2,3,4,9,9-hexachloro-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2OC2C(=O)C2C1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74972
1,2,3,4,9,9-hexachloro-6,7-epoxy-1,4,4a,6,7,8a-hexahydro-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1=CC(=O)C2C(C1=O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74973
1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-6-methyl-1,4-methanonaphthalene-5,8-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1CCC2C(C1)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74975
crude adduct
DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ