79815-20-6
- Product Name：(S)-(-)-indoline-2-carboxylic acid
- Molecular Formula：C9H9NO2
- Purity：99%
- Molecular Weight：163.176
Product Details;
CasNo： 79815-20-6
Molecular Formula： C9H9NO2
Appearance： white to light yellow crystal powder
Quality Factory Supply (S)-(-)-indoline-2-carboxylic acid, Export 79815-20-6 with Cheapest Price
- Molecular Formula:C9H9NO2
- Molecular Weight:163.176
- Appearance/Colour:white to light yellow crystal powder
- Vapor Pressure:1.88E-06mmHg at 25°C
- Melting Point:177 °C (dec.)(lit.)
- Refractive Index:-116 ° (C=1, 2mol/L HCl)
- Boiling Point:380 °C at 760 mmHg
- PKA:2.04±0.20(Predicted)
- Flash Point:183.6 °C
- PSA：49.33000
- Density:1.286 g/cm3
- LogP:1.24580
(S)-(-)-indoline-2-carboxylic acid (Cas 79815-20-6) Usage
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Chemical Properties |
white to light yellow crystal powde |
| Description | (S)-(-)-Indoline-2-carboxylic acid is a chemical compound primarily used as a catalyst for enantioselective cyclopropanations. It is known for its ability to facilitate chemical reactions with high enantioselectivity. (S)-(-)-Indoline-2-carboxylic acid can be obtained from various chemical suppliers, including Santa Cruz, Sigma-Aldrich, and LGC Standards. |
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Uses |
Catalyst for enantioselective cyclopropanations. (S)-(-)-Indoline-2-carboxylic acid can be used as a catalyst in palladium-catalyzed cyclization reactions, which are important in the synthesis of various organic compounds. It plays a role in the preparation of spirooxindole-pyrrolidones. |
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Consumer Uses |
ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment. |
InChI:InChI=1/C9H9NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h1-4,8,10H,5H2,(H,11,12)/t8-/m1/s1
79815-20-6 Relevant articles
Semi-rational protein engineering of a novel esterase from Bacillus aryabhattai (BaCE) for resolution of (R,S)-ethyl indoline-2-carboxylate to prepare (S)-indoline-2-carboxylic acid
Zhang, Hongjun,Cheng, Zeguang,Wei, Litian,Yu, Xinjun,Wang, Zhao,Zhang, Yinjun
, (2022/01/24)
A gene encoding an esterase from Bacillu...
Spectroscopy and Photophysics of Indoline and Indoline-2-Carboxylic Acid
Michael W. Allen, Jay R. Unruh, Brian D. Slaughter, Sarah J. Pyszczynski, Thaddaus R. Hellwig, Tim J. Kamerzell, and Carey K. Johnson
, J. Phys. Chem. A 2003, 107, 30, 5660–5669
The (S)-(−)-indoline-2-carboxylic acid isomer retains the same stereochemistry as the l-amino acids.
Characterization of an enantioselective amidase from Cupriavidus sp. KNK-J915 (FERM BP-10739) useful for enzymatic resolution of racemic 3-piperidinecarboxamide
Nojiri, Masutoshi,Taoka, Naoaki,Yasohara, Yoshihiko
, p. 136 - 142 (2014/12/10)
A novel amidase (CsAM) acting on (R,S)-N...
79815-20-6 Process route
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indoline-2-carboxylic acid (R)-α-methylbenzylamine salt
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- 79815-20-6,78348-24-0
(S)-indoline-2-carboxylic acid
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- 98167-06-7,78348-24-0
(R)-(-)-2,3-Dihydro-1H-Indole-2-Carboxylic Acid
| Conditions | Yield |
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With hydrogenchloride; In water; for 2h;
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- 79815-20-6,78348-24-0
(S)-indoline-2-carboxylic acid
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- 98167-06-7,78348-24-0
(R)-(-)-2,3-Dihydro-1H-Indole-2-Carboxylic Acid
| Conditions | Yield |
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79815-20-6 Upstream products
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82950-72-9
1-acetyl-2,3-indoline-2-carboxylic acid
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78779-29-0
l-(S)-2,3-dihydro-1-[(S)-3-mercapto-2-methyl-1-oxopropyl]-1H-indole-2-carboxylic acid
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496790-47-7
1-benzhydryl-2,3-dihydro-1H-indole-2-carboxylic acid tert-butyl ester
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496790-43-3
2-(benzhydrylidene-amino)-3-(2-bromo-phenyl)-propionic acid tert-butyl ester
79815-20-6 Downstream products
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141410-06-2
(S)-indoline-2-carboxylic acid methyl ester
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82923-81-7
(S)-2,3-dihydro-1H-indole-2-carboxylic acid ethyl ester
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79854-42-5
Ethyl (S)-indoline-2-carboxylate hydrochloride
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80875-98-5
(2S,3aS,7aS)-perhydroindole-2-carboxylic acid
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