page_banner

product

(S)-Indoline-2-carboxylic Acid(CAS# 79815-20-6)

Chemical Property:

Molecular Formula C9H9NO2
Molar Mass 163.17
Density 1.2021 (rough estimate)
Melting Point 177°C (dec.)(lit.)
Boling Point 290.25°C (rough estimate)
Specific Rotation(α) -112.5 º (c=1, 1N HCl)
Flash Point 183.6°C
Water Solubility Slightly soluble in water
Vapor Presure 1.88E-06mmHg at 25°C
Appearance Light Yellow Crystal
Color Beige to brown
pKa 2.04±0.20(Predicted)
Storage Condition Keep in dark place,Inert atmosphere,2-8°C
Refractive Index -116 ° (C=1, 2mol/L
MDL MFCD00070578
Physical and Chemical Properties Melting point 177°C (dec.)
specific optical rotation -112.5 ° (c = 1, 1N HCl)
Use The intermediate of the new drug-Puli is mainly used to treat cardiovascular and cerebrovascular diseases.

Product Detail

Product Tags

Hazard Symbols Xn – Harmful
Risk Codes R43 – May cause sensitization by skin contact
R48/22 – Harmful danger of serious damage to health by prolonged exposure if swallowed.
R62 – Possible risk of impaired fertility
Safety Description S22 – Do not breathe dust.
S25 – Avoid contact with eyes.
S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37 – Wear suitable protective clothing and gloves.
WGK Germany 2
HS Code 29339900

 

Introduction

(S)-(-)-Indoline-2-carboxylic acid, chemically known as (S)-(-)-Indoline-2-carboxylic acid, is an organic compound.

 

Quality:

(S)-(-)-indolin-2-carboxylic acid is a colorless crystal with special structural and chiral characteristics. It has two stereoisomers, which are (S)-(-)-indolin-2-carboxylic acid and (R)-(+)-indoldoline-2-carboxylic acid.

 

Use:

(S)-(-)-indolin-2-carboxylic acid is widely used in organic synthesis. It is an important intermediate in the preparation of indoline compounds. It is also commonly used in the preparation of catalysts and stereoisomers for chiral synthesis.

 

Method:

(S)-(-)-indolin-2-carboxylic acid can usually be prepared by chiral synthesis. A common method is to use chiral derivatives for asymmetric reactions, such as asymmetric Yongji-Bodhi oxidation of pyridine using a chiral denitrification catalyst to obtain (S)-(-)-indolline-2-carboxylic acid.

 

Safety Information:

(S)-(-)-Indoline-2-carboxylic acid has low toxicity under conventional operating conditions. However, as an organic compound, it can have an irritating effect on the skin, eyes, and respiratory tract, and direct contact should be avoided and good ventilation should be maintained. Laboratory safety operating procedures should be strictly adhered to, and the compound should be stored and handled properly. In any case, it should be avoided by ingesting or inhaling. In case of skin contact or inhalation, wash immediately or call first aid.


  • Previous:
  • Next:

  • Write your message here and send it to us