Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H12O4 |
| Molecular Weight | 160.1678 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(CC)(C(O)=O)C(O)=O
InChI
InChIKey=LTMRRSWNXVJMBA-UHFFFAOYSA-N
InChI=1S/C7H12O4/c1-3-7(4-2,5(8)9)6(10)11/h3-4H2,1-2H3,(H,8,9)(H,10,11)
| Molecular Formula | C7H12O4 |
| Molecular Weight | 160.1678 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and biological activities of novel structural analogues of 2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand. | 2001 Aug 6 |
|
| N-(3-Acyloxy-2-benzylpropyl)-N'-(4-hydroxy-3-methoxybenzyl) thiourea derivatives as potent vanilloid receptor agonists and analgesics. | 2001 Jan |
|
| X-H (X = C, N, O, P, S) bond activations induced by beta-heterosubstituted zirconaindenes. | 2001 Jan 5 |
|
| Effect of malonyl malonanilide dimers on the thermal stability of nitrocellulose. | 2001 Nov 16 |
|
| A general and mild copper-catalyzed arylation of diethyl malonate. | 2002 Jan 24 |
|
| Palladium-catalyzed arylation of malonates and cyanoesters using sterically hindered trialkyl- and ferrocenyldialkylphosphine ligands. | 2002 Jan 25 |
|
| Novel autoxidation and Michael addition of a butenolide-containing sugar leading to a C-branched-chain glucopyranosidulose, and X-ray structure of intermediates. | 2003 Aug 12 |
|
| Formal synthesis of angiogenesis inhibitor NM-3. | 2003 Jul 25 |
|
| Probing the electrostatic shielding of DNA with capillary electrophoresis. | 2003 Mar |
|
| Synthesis and evaluation of 2,6-piperidinedione derivatives as potentially novel compounds with analgesic and other CNS activities. | 2006 Mar |
|
| tert-Butyl 3-[2,2-bis-(ethoxy-carbon-yl)-vinyl]-2-methyl-1H-indole-1-carboxyl-ate. | 2009 Mar 25 |
|
| Diethyl 2-[(5-meth-oxy-2-methyl-1-phenyl-sulfonyl-1H-indol-3-yl)methyl-ene]malonate. | 2009 May 29 |
|
| (3aR*,7aS*)-1-(p-Tolyl-sulfon-yl)perhydro-indol-2-one. | 2010 Apr 17 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:18:42 GMT 2023
by
admin
on
Sat Dec 16 04:18:42 GMT 2023
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| Record UNII |
QHT44LOC3W
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| Record Status |
Validated (UNII)
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| Record Version |
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m4410
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1986
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C030978
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