ChemicalBook > CAS DataBase List > (S)-(-)-Indoline-2-carboxylic acid

(S)-(-)-Indoline-2-carboxylic acid

Product Name
(S)-(-)-Indoline-2-carboxylic acid
CAS No.
79815-20-6
Chemical Name
(S)-(-)-Indoline-2-carboxylic acid
Synonyms
Indoline-2-carboxylic acid;(R)-2,3-DIHYDRO-1H-INDOLE-2-CARBOXYLIC ACID;H-Idc-OH;H-L-Idc-OH;S)-(-)-Indoline-2-ca;Perindopril Impurity 48;Perindopril Impurity 46;Perindopril Impurity 40;Perindopril Intermediate;S-Indoline-2-Formic acid
CBNumber
CB2235455
Molecular Formula
C9H9NO2
Formula Weight
163.17
MOL File
79815-20-6.mol
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(S)-(-)-Indoline-2-carboxylic acid Property

Melting point:
177 °C (dec.)(lit.)
alpha 
-112.5 º (c=1, 1N HCl)
Boiling point:
290.25°C (rough estimate)
Density 
1.2021 (rough estimate)
refractive index 
-116 ° (C=1, 2mol/L HCl)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
Water Solubility 
Slightly soluble in water
pka
2.04±0.20(Predicted)
form 
Powder
color 
Beige to brown
optical activity
[α]20/D 114°, c = 1 in 1 M HCl
InChI
InChI=1S/C9H9NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h1-4,8,10H,5H2,(H,11,12)/t8-/m0/s1
InChIKey
QNRXNRGSOJZINA-QMMMGPOBSA-N
SMILES
N1C2=C(C=CC=C2)C[C@H]1C(O)=O
CAS DataBase Reference
79815-20-6(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
43-48/22-62
Safety Statements 
22-25-26-36/37
WGK Germany 
2
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H317May cause an allergic skin reaction

H373May cause damage to organs through prolonged or repeated exposure

Precautionary statements

P202Do not handle until all safety precautions have been read and understood.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P272Contaminated work clothing should not be allowed out of the workplace.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P308+P313IF exposed or concerned: Get medical advice/attention.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
346802
Product name
(S)-(?)-Indoline-2-carboxylic acid
Purity
99%
Packaging
1g
Price
$68.8
Updated
2025/07/31
Sigma-Aldrich
Product number
346802
Product name
(S)-(?)-Indoline-2-carboxylic acid
Purity
99%
Packaging
5g
Price
$219
Updated
2025/07/31
TCI Chemical
Product number
I0395
Product name
(S)-(-)-Indoline-2-carboxylic Acid
Purity
>95.0%(T)
Packaging
1g
Price
$27
Updated
2025/07/31
TCI Chemical
Product number
I0395
Product name
(S)-(-)-Indoline-2-carboxylic Acid
Purity
>95.0%(T)
Packaging
5g
Price
$80
Updated
2025/07/31
TRC
Product number
I627213
Product name
(S)-(?)-Indoline-2-carboxylic acid
Packaging
100mg
Price
$45
Updated
2021/12/16
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(S)-(-)-Indoline-2-carboxylic acid Chemical Properties,Usage,Production

Chemical Properties

white to light yellow crystal powde

Uses

Catalyst for enantioselective cyclopropanations.

Synthesis

42538-40-9

79815-20-6

Example 1 Synthesis of (S)-2,3-dihydro-1H-indole-2-carboxylic acid: In a 100 mL flask, 366 mg (1.5 mmol) of (S)-2-bromophenylalanine, 217 mg (1.6 mmol) of K2CO3, 3.2 mg (0.03 mmol) of CuCl, and 3.2 g of N-methyl pyrrolidone (NMP) were added in order. ). The reactor was flushed with argon and kept under a slow flow of argon. The reaction mixture was stirred and heated to 100 °C, which was maintained. Samples were taken periodically and analyzed by high performance liquid chromatography (HPLC). after 4 h, (S)-2-bromophenylalanine was completely converted to the target product. (The yield (in solution) of (S)-2,3-dihydro-1H-indole-2-carboxylic acid was 95.9% with an enantiomeric excess (ee) > 98.6%. Example 2 Synthesis of (S)-2,3-dihydro-1H-indole-2-carboxylic acid: 9.76 g (40.0 mmol) of (S)-2-bromophenylalanine, 5.80 g (42.0 mmol) of K2CO3, 40 mg (0.4 mmol) of CuCl, and 40 g of NMP were sequentially added to a flask at 80 °C. The reactor was flushed with argon and then kept under a slow flow of argon. The reaction mixture was stirred and heated to 80 °C, which was maintained. Samples were taken periodically and analyzed by HPLC. after 3.5 h, (S)-2-bromophenylalanine was completely converted. The reaction mixture was cooled to 25 °C, followed by the addition of 40 mL of water and 50 mL of ethyl acetate (EtOAc). The pH of the mixture was adjusted to 3.3 with 3.5 g of a 37% aqueous hydrochloric acid solution. after separation of the phases, the aqueous phase was extracted with 2 x 50 mL of EtOAc. The combined organic layers were washed with 25 mL of saturated aqueous sodium chloride and the organic phase was subsequently concentrated. The residue was dissolved in 16 mL of aqueous 5N hydrochloric acid, and the pH was adjusted to 2.1 with 9.4 g of 32% aqueous sodium hydroxide. the precipitated (S)-2,3-dihydro-1H-indole-2-carboxylic acid was separated by filtration and washed with 2 x 10 mL of water. After drying, 3.24 g (19.8 mmol) of (S)-2,3-dihydro-1H-indole-2-carboxylic acid was obtained in 49.5% yield, ee > 99%.

References

[1] Patent: EP1676838, 2006, A1. Location in patent: Page/Page column 16
[2] Patent: EP1676838, 2006, A1. Location in patent: Page/Page column 17
[3] Journal of Organic Chemistry, 2014, vol. 79, # 17, p. 7872 - 7879
[4] Patent: EP1676838, 2006, A1. Location in patent: Page/Page column 16-17
[5] Patent: WO2006/69799, 2006, A1. Location in patent: Page/Page column 28-29

(S)-(-)-Indoline-2-carboxylic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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(S)-(-)-Indoline-2-carboxylic acid Suppliers

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View Lastest Price from (S)-(-)-Indoline-2-carboxylic acid manufacturers

ShenZhen H&D Pharmaceutical Technology Co., LTD
Product
Perindopril Impurity 40 79815-20-6
Price
US $0.00-0.00/mg
Min. Order
10mg
Purity
98%
Supply Ability
500mg
Release date
2024-08-07
ShenZhen H&D Pharmaceutical Technology Co., LTD
Product
Perindopril Impurity 46
Price
US $0.00-0.00/mg
Min. Order
10mg
Purity
98%
Supply Ability
500mg
Release date
2024-08-08
Hebei Chuanghai Biotechnology Co,.LTD
Product
(S) - (-) -Indoline-2-Carboxylic Acid 79815-20-6
Price
US $5.00-2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-23

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  • CARBOXYLIC ACID
  • Proline-Based Organocatalysts
  • Chiral Catalysts, Ligands, and Reagents
  • Asymmetric Synthesis
  • Heterocycle-Indole series
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