Weight | 129.159 g/mol |
---|---|
Formula | C6H11NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
1-methyl-D-Proline (58123-62-9)
68078-09-1 · 1-methyl-L-proline · 475-11-6
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- Stereochemical Studies. XXXVIII. Asymmetric Synthesis of the Key Compounds for the Synthesis of optically Active Diterpenes. Asymmetric Synthesis of optically Active 1,2,3,4,5,6,7,8,8a-Octahydro-8a-methyl-3,8-naphthalenedione Derivatives with L-Proline Derivatives (Chemical & Pharmaceutical Bulletin, 1975)
- Catalysis of the Covalent Binding of 3-Hydroxyamino-1-methyl-5H-pyrido[4,3-b]indole to DNA by a l-Proline- and Adenosine Triphosphate-dependent Enzyme in Rat Hepatic Cytosol (Cancer Research, 1985)
- Urinary metabolites of 1-(3-Mercapto-2-D-methyl-1-oxopropyl)-L-proline(SQ-14225),a new antihypertensive agent, in rats and dogs. (Chemical & Pharmaceutical Bulletin, 1981)
- L-Proline-Catalyzed Activation of Methyl Ketones or Active Methylene Compounds and DMF-DMA for Syntheses of (2E)-3-Dimethylamino-2- propen-1-ones (European Journal of Organic Chemistry, 2012)
- L-proline-catalyzed 1,3-dipolar cycloaddition of some Schiff bases to methyl 4-[1-oxo-2-(2-oxo-2,3-dihydro-1H-indol-3-ylidene)ethyl]phenylcarbamate (Russian Journal of Organic Chemistry, 2011)
- The synthesis of SQ-14225-14C [N-[(S)-2-methyl-3-mercaptopropanoyl-1-14C]-L-proline] (Journal of Labelled Compounds and Radiopharmaceuticals, 1981)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 68078-09-1
- 1-methyl-L-proline
- 475-11-6
- 1-methylproline
-
SMILESCN1CCCC1C(=O)O
-
InChIKeyCWLQUGTUXBXTLF-UHFFFAOYSA-N
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Alternate Names
Estimated Properties
Boiling Point | 215.95 C | EPA T.E.S.T. |
---|---|---|
Boiling Point | 408.98 C | EPI Suite |
Density | 1.1 g/cm3 | EPA T.E.S.T. |
Flash Point | 99.48 C | EPA T.E.S.T. |
Melting Point | 284.69 C | EPI Suite |
Water Solubility | 156522 mg/L | EPA T.E.S.T. |
Water Solubility | 65366 mg/L | EPI Suite |
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