بحث البنية الفرعية

COCCOC

O=C1CCCCCO1.O=C1COCCO1
Reaction #2356
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2357
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2358
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCCO1.O=C1COCCO1
Reaction #2359
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@H]1COC[C@H]1OC(=O)C(C)Cl
Reaction #3176
(±)-(3R,4S)-4-Acetoxy-3-(2-chloropropionyloxy)tetrahydrofuran
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC1CO1
Reaction #5687
glycidyl methacrylate
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCOc1ccc(C[C@H](NC(=O)OC(C)(C)C)C(=O)OC)cc1
Reaction #5822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOC(=O)C1CC1
Reaction #7072
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1ccc(N2C[C@H](CO)OC2=O)cc1F
Reaction #8250
title compound
المردود 44.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn(-c2ccc(N3C[C@H](CO)OC3=O)cc2F)cn1
Reaction #8254
title product
المردود 33.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](O)CSCc1ccccc1
Reaction #43569
(R)-3-Benzylsulfanyl-2-hydroxy-propionic acid methyl ester
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(C)OC(=O)C(C)C
Reaction #50361
propylene glycol monomethyl ether iso-butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CN=C([C@H](C)NC(=O)Cc2cc(F)cc(F)c2)O1
Reaction #51294
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOCCOC(=O)CCC(C)=O
Reaction #54170
2-Butoxyethyl Levulinate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NO)c1ccc2c(c1O)OC(CO)CO2
Reaction #56745
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc3c(c2o1)OC(CO)CO3
Reaction #56746
[2-Methyl-7,8-dihydro[1,4]dioxino[2,3-g][1,3]benzoxazol-8-yl]methanol
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OCC1CO1.C=CC(=O)OCCCC
Reaction #71315
copolymer ( B8 )
DOI: 10.6084/m9.figshare.5104873.v1
CN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73939
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C(C)=C/c1cc(F)c(Oc2ccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])cc2)c(F)c1
Reaction #73969
title compound
المردود 47.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN1Cc2c(Cl)cc(Cl)cc2C(c2cccc(S(=O)(=O)NCCOCCOCCOCCN=[N+]=[N-])c2)C1
Reaction #73990
N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-3-(6,8-dichloro-2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide
المردود 55.4%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي