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MISSION shRNA-RNAi
MISSION siRNA
Molecular Formula
CAS No.
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Description
Molecular Formula
Product #
(
R
)-(+)-Methyl (
R
)-2-chloropropionate 98%
C
4
H
7
ClO
2
277754
(−)-Methyl (
S
)-2-chloropropionate purum, ≥97.0% (sum of enantiomers, GC)
C
4
H
7
ClO
2
26222
(−)-Methyl (
S
)-2-chloropropionate 99%
C
4
H
7
ClO
2
247030
(−)-Methyl
L
-lactate 98%, optical purity ee: 97% (GLC)
C
4
H
8
O
3
230340
(−)-Methyl
L
-lactate purum, ≥95.0% (sum of enantiomers, GC)
C
4
H
8
O
3
69809
(+)-Methyl
D
-lactate 98%, optical purity ee: 96% (GLC)
C
4
H
8
O
3
277762
(−)-Methyl (
S
)-3-bromo-2-
methylpropionate purum, ≥95.0% (sum of enantiomers, GC)
C
5
H
9
BrO
2
17621
Methyl (
R
)-(+)-3-bromo-2-
methylpropionate 97%
C
5
H
9
BrO
2
325090
(−)-Methyl (
S
)-3-bromo-2-
methylpropionate 97%
C
5
H
9
BrO
2
324922
(+)-Methyl (R)-3-bromo-2-
methylpropionate purum, ≥95.0% (sum of enantiomers, GC)
C
5
H
9
BrO
2
17616
(+)-Methyl (S)-3-hydroxybutyrate puriss., ≥99.0% (sum of enantiomers, GC)
C
5
H
10
O
3
54958
Methyl (
S
)-(+)-3-
hydroxybutyrate 99%
C
5
H
10
O
3
243167
(−)-Methyl
D
-β-
hydroxyisobutyrate purum, ≥98.0% (sum of enantiomers, GC)
C
5
H
10
O
3
55415
Methyl (
R
)-(−)-3-
hydroxy-2-methylpropionate 99%
C
5
H
10
O
3
270148
Methyl (
S
)-(+)-3-hydroxy-2-
methylpropionate 99%
C
5
H
10
O
3
270121
(+)-Methyl
L
-β-
hydroxyisobutyrate purum, ≥95.0% (sum of enantiomers, GC)
C
5
H
10
O
3
55412
(−)-Ethyl
L
-lactate purum, ≥98.0% (sum of enantiomers, GC)
C
5
H
10
O
3
69799
(−)-Ethyl
L
-lactate 98%
C
5
H
10
O
3
E34102
(+)-Ethyl
D
-lactate puriss., ≥99.0% (sum of enantiomers, GC)
C
5
H
10
O
3
69796
Methyl (
R
)-3-hydroxybutyrate puriss., ≥99.0% (sum of enantiomers, GC)
C
5
H
10
O
3
54957
Methyl (
R
)-3-hydroxybutyrate 99%
C
5
H
10
O
3
243159
Dimethyl (4S,5S)-1,3,2-dioxathiolane-
4,5-dicarboxylate 2,2-dioxide purum
C
6
H
8
O
8
S
42544
Dimethyl (4
R
,5
R
)-1,3,2-
dioxathiolane-4,5-
dicarboxylate 2,2-dioxide 97%
C
6
H
8
O
8
S
441015
Ethyl (
R
)-(+)-4,4,4-
trifluoro-3-hydroxybutyrate 99%
C
6
H
9
F
3
O
3
376795
Ethyl (
R
)-2-
(trifluoromethylsulfonyloxy)propionate purum, ≥97.0% (
19
F-NMR)
C
6
H
9
F
3
O
5
S
91724
Ethyl (
S
)-2-
(trifluoromethylsulfonyloxy)propionate ≥96%
C
6
H
9
F
3
O
5
S
374636
(
R
)-(+)-2-
Methylsuccinic acid 4-methyl ester 95%
C
6
H
10
O
4
546720
Dimethyl (
R
)-(+)-malate 98%
C
6
H
10
O
5
455040
Dimethyl
D
-malate puriss., ≥99.0% (sum of enantiomers, GC)
C
6
H
10
O
5
02318
Dimethyl
L
-malate puriss., ≥99.0% (sum of enantiomers, GC)
C
6
H
10
O
5
02315
Dimethyl (
S
)-(−)-malate 98%
C
6
H
10
O
5
374318
(+)-Dimethyl
L
-tartrate purum, ≥99.0% (sum of enantiomers, GC)
C
6
H
10
O
6
95365
(−)-Dimethyl
D
-tartrate 99%
C
6
H
10
O
6
242942
(+)-Dimethyl
L
-tartrate 99%
C
6
H
10
O
6
163457
Ethyl (
S
)-(−)-4-bromo-
3-hydroxybutyrate technical grade
C
6
H
11
BrO
3
479608
Ethyl (
R
)-(+)-4-bromo-3-
hydroxybutyrate technical grade
C
6
H
11
BrO
3
542911
Ethyl (
R
)-(+)-4-chloro-3-
hydroxybutyrate 96%
C
6
H
11
ClO
3
460516
Ethyl (
S
)-(−)-4-
chloro-3-hydroxybutyrate 96%
C
6
H
11
ClO
3
460524
Ethyl (
S
)-(−)-4-
chloro-3-hydroxybutyrate purum, ≥95.0% (GC)
C
6
H
11
ClO
3
94893
(−)-Isopropyl
L
-lactate purum, ≥97.0% (sum of enantiomers, GC)
C
6
H
12
O
3
69807
Ethyl (
S
)-3-hydroxybutyrate 99%
C
6
H
12
O
3
374709
(+)-Methyl (
S
)-3-hydroxyvalerate purum, ≥98.0% (sum of enantiomers, GC)
C
6
H
12
O
3
56657
(−)-Methyl (
R
)-3-hydroxyvalerate purum, ≥98.0% (sum of enantiomers, GC)
C
6
H
12
O
3
56655
Ethyl (
S
)-3-hydroxybutyrate puriss., ≥98.5% (sum of enantiomers, GC)
C
6
H
12
O
3
54955
Ethyl (
R
)-(−)-3-
hydroxybutyrate 98%
C
6
H
12
O
3
347329
Ethyl (
R
)-(−)-4-cyano-
3-hydroxybutyrate 95%
C
7
H
11
NO
3
479772
Dimethyl (
R
)-(+)-
methylsuccinate 99%
C
7
H
12
O
4
382094
(−)-Methyl (
S
)-2,2-dimethyl-1,3-
dioxolane-4-carboxylate 96%
C
7
H
12
O
4
254606
Methyl (
R
)-(+)-2,2-dimethyl-
1,3-dioxolane-4-carboxylate 98%
C
7
H
12
O
4
345482
Isobutyl (S)-2-chloropropionate puriss., ≥99.0% (sum of enantiomers, GC)
C
7
H
13
ClO
2
51401
Isobutyl (
R
)-(+)-lactate 97%
C
7
H
14
O
3
316598
(−)-Butyl
L
-lactate purum, ≥97.0% (sum of enantiomers, GC)
C
7
H
14
O
3
69819
(+)-Isobutyl
D
-lactate puriss., ≥99.0% (sum of enantiomers, GC)
C
7
H
14
O
3
69815
(+)-
tert
-Butyl
D
-lactate puriss., ≥99.0% (sum of enantiomers, GC)
C
7
H
14
O
3
69806
Ethyl (1
R
,2
S
)-
cis
-2-
hydroxycyclopentanecarboxylate purum, ≥97.0% (GC)
C
8
H
14
O
3
