propylene glycol

C[C@@H]1OC(=O)[C@H](C)OC1=O.O=C1CCCCCO1
Reaction #2355
ε-CAPROLACTONE L-LACTIDE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCCCO1.O=C1COCCO1
Reaction #2357
ε-CAPROLACTONE p-DIOXANONE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCCCO1.O=C1OCCCO1
Reaction #2360
ε-CAPROLACTONE TRIMETHYLENE CARBONATE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCCCO1.O=C1OCCCO1
Reaction #2361
ε-CAPROLACTONE TRIMETHYLENE CARBONATE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(CO[Si](C)(C)C)O[Si](C)(C)C
Reaction #5153
colorless oil
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(O)COC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #8582
title compound
収率 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1COc2cscc2O1
Reaction #10705
Racemic 2-methyl-2,3-dihydro-thieno[3,4-b][1,4]dioxine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1COC(C)(c2ccc(S(=O)(=O)Nc3ccc(Cl)cc3C(=O)c3ccncc3)cc2)O1
Reaction #57805
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1COC(c2nsc3ccc(-n4c(=O)cc(C(F)(F)F)n(C)c4=O)cc23)O1
Reaction #77284
title compound
収率 87.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC1=CC2(CC(C)(C)C1=O)OCC(C)O2
Reaction #94328
product
収率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CC1CO1
Reaction #96135
propylene oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(O)CO.CCCC=O
Reaction #161303
n-Butyraldehyde 1,2-Propanediol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCN(CCC)c1c([N+](=O)[O-])cc(C2OCC(C)O2)cc1[N+](=O)[O-]
Reaction #175646
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(-c2c(-c3ccccc3)oc3ncnc(OC(C)CO)c23)cc1
Reaction #192066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CC(c1cccc(Cl)c1)C(N)c1ccc(Cl)cc1
Reaction #193554
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1C(=O)N(c2cc(Cl)cc(Cl)c2)C(=O)[C@]12CN(Cc1cc(C(=O)O)cs1)C[C@H]2c1ccc(C#N)cc1
Reaction #217552
5-[(5S,9R)-9-(4-Cyanophenyl)-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non-7-ylmethyl]-thiophene-3-carboxylic acid
収率 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
COCC(O)CN(C(C)=O)c1c(I)c(C(=O)NCC(O)CO)c(I)c(C(=O)NCC(O)CO)c1I
Reaction #263335
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(O)COC(=O)c1ccccc1
Reaction #265880
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCCCCCCCCCCCCCCCNc1ccc(C(=O)OCC(C)O)cc1
Reaction #270843
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1Nc2cccc(C=Cc3ccc(O)cc3)c2C1=O
Reaction #289110
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
1 ページ次のページ