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Plant Sources
Structural Classes
Microbial Sources
Flagship Varieties
Synthetic Compounds
All
CAS No.
NAME
Molecular Formula
Molecular Weight
Purity
Price
2D Structure
1246833-97-5
Zuclopenthixol-d4 Succinate Salt
C1CN(CCN1CCC=C2C3=CC=CC=C3SC4=C2C=C(C=C4)Cl)CCO.C(CC(=O)O)C(=O)O
C
26
H
31
ClN
2
O
5
S
523.1
-
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159811-51-5
Ulipristal
CC(=O)C1(CCC2C1(CC(C3=C4CCC(=O)C=C4CCC23)C5=CC=C(C=C5)N(C)C)C)O
C
28
H
35
NO
3
433.6
-
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1216989-17-1
D 13223-d4 (Flupirtine Metabolite)
CC(=O)NC1=C(N=C(C=C1)NCC2=CC=C(C=C2)F)N.Cl
C
14
H
16
ClFN
4
O
314.78
-
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1217632-04-6
CID 137245734
C1=C(N=C2C(=O)NC(=NC2=N1)N)C(C(CO)O)O
C
9
H
11
N
5
O
4
258.18
95%
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1216451-53-4
rac Ketorolac-d4
C1CN2C(=CC=C2C(=O)C3=CC=CC=C3)C1C(=O)O
C
15
H
13
NO
3
259.29
-
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127413-31-4
Flecainide-d3
C1CCNC(C1)CNC(=O)C2=C(C=CC(=C2)OCC(F)(F)F)OCC(F)(F)F
C
17
H
20
F
6
N
2
O
3
417.36
-
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1217838-71-5
Biopterin-d3
CC(C(C1=CN=C2C(=N1)C(=O)NC(=N2)N)O)O
C
9
H
11
N
5
O
3
240.23
-
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1329796-98-6
D,L-Mevalonic Acid-d3 Dicyclohexylamine Salt
CC(CCO)(CC(=O)O)O.C1CCC(CC1)NC2CCCCC2
C
18
H
35
NO
4
332.5
-
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1215511-11-7
N-Methyl-4-aminobutyric Acid-d3
CNCCCC(=O)O
C
5
H
11
NO
2
120.16
-
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285977-83-5
Thiourea-13C,15N2
C(=S)(N)N
CH
4
N
2
S
79.10
-
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1246833-97-5
Zuclopenthixol-d4 Succinate Salt
Zuclopenthixol
C
26
H
31
ClN
2
O
5
S
523.1
159811-51-5
Ulipristal
醋酸乌利司他中间体
C
28
H
35
NO
3
433.6
1216989-17-1
D 13223-d4 (Flupirtine Metabolite)
D 13223-d4 (Flupirtine Metabolite)
C
14
H
16
ClFN
4
O
314.78
1217632-04-6
CID 137245734
D-Neopterin-13C5
C
9
H
11
N
5
O
4
258.18
1216451-53-4
rac Ketorolac-d4
rac Ketorolac-d4
C
15
H
13
NO
3
259.29
127413-31-4
Flecainide-d3
Flecainide-d3
C
17
H
20
F
6
N
2
O
3
417.36
1217838-71-5
Biopterin-d3
Biopterin-d3
C
9
H
11
N
5
O
3
240.23
1329796-98-6
D,L-Mevalonic Acid-d3 Dicyclohexylamine Salt
D,L-Mevalonic Acid-d3 Dicyclohexylamine Salt
C
18
H
35
NO
4
332.5
1215511-11-7
N-Methyl-4-aminobutyric Acid-d3
N-Methyl-4-aminobutyric Acid-d3
C
5
H
11
NO
2
120.16
285977-83-5
Thiourea-13C,15N2
Thiourea-13C,15N2
CH
4
N
2
S
79.10
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