80875-98-5

  • Product Name:(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid
  • Molecular Formula:C9H15NO2
  • Purity:99%
  • Molecular Weight:169.224
Inquiry

Product Details;

CasNo: 80875-98-5

Molecular Formula: C9H15NO2

Appearance: White solid

Factory Supply High Purity Top 99% 80875-98-5 (2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid On Stock

  • Molecular Formula:C9H15NO2
  • Molecular Weight:169.224
  • Appearance/Colour:White solid 
  • Vapor Pressure:7.54E-05mmHg at 25°C 
  • Melting Point:275-277 °C 
  • Refractive Index:1.507 
  • Boiling Point:318.6 °C at 760 mmHg 
  • PKA:2.47±0.20(Predicted) 
  • Flash Point:146.5 °C 
  • PSA:49.33000 
  • Density:1.135 g/cm3 
  • LogP:1.32050 

(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid (Cas 80875-98-5) Usage

Chemical Properties

White Solid

Uses

(2S,3aS,7aS)-Octahydro-1H-indole-2-carboxylic acid can be used as An intermediate in the synthesis of Perindopril. Perindopril USP Related Compound A.

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/C9H15NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h6-8,10H,1-5H2,(H,11,12)/t6-,7-,8-/m0/s1

80875-98-5 Relevant articles

Separation and quantification of octahydro-1h-indole-2-carboxilic acid and its three isomers by HPLC using refractive index detector

SJ Vali, SS Kumar, SS Sait, LK Garg

, J Chromat Separation Techniq, 2012

In the current study (2S,3aS,7aS)-octahydro-1H-indole-2-carboxylic acid was used as a raw material for Perindopril and quantified the purity of raw material as well as quantified the …

Practical access to the proline analogs (S,S,S)- and (R,R,R)-2- methyloctahydroindole-2-carboxylic acids by HPLC enantioseparation

Sayago, Francisco J.,Pueyo, Maria J.,Calaza, M. Isabel,Jimenez, Ana I.,Cativiela, Carlos

scheme or table, p. 507 - 513 (2012/01/11)

An efficient methodology for the prepara...

Highly Enantioselective Inverse‐Electron‐Demand Hetero‐Diels–Alder Reactions Catalyzed by Modularly Designed Organocatalysts

D Sinha, S Perera, JCG Zhao

, Chemistry–A European Journal, 2013

Proline and (2S,3aS,7aS)-octahydro-1H-indole-2-carboxylic acid are both poor catalysts for the inverse-electron-demand hetero-Diels–Alder reactions between aldehydes and electron-…

80875-98-5 Process route

indolin-2-yl carboxylic acid
16851-56-2,78348-24-0

indolin-2-yl carboxylic acid

(+/-)-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid
80828-13-3,80875-98-5,82717-40-6,87679-20-7,87679-39-8,87679-51-4,87679-58-1,88547-85-7,88585-94-8,96844-78-9,108507-42-2,145438-94-4,145438-95-5,145513-90-2,145513-91-3,145513-92-4,145513-93-5,2055118-14-2

(+/-)-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid

(+/-)-(2R,3aS,7aS)-octahydroindole-2-carboxylic acid
80828-13-3,80875-98-5,82717-40-6,87679-20-7,87679-39-8,87679-51-4,87679-58-1,88547-85-7,88585-94-8,96844-78-9,108507-42-2,145438-94-4,145438-95-5,145513-90-2,145513-91-3,145513-92-4,145513-93-5,2055118-14-2

(+/-)-(2R,3aS,7aS)-octahydroindole-2-carboxylic acid

Conditions
Conditions Yield
With hydrogen; acetic acid; platinum(IV) oxide; at 60 ℃; for 24h;
70%
indolin-2-yl carboxylic acid
16851-56-2,78348-24-0

indolin-2-yl carboxylic acid

(+/-)-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid
80828-13-3,80875-98-5,82717-40-6,87679-20-7,87679-39-8,87679-51-4,87679-58-1,88547-85-7,88585-94-8,96844-78-9,108507-42-2,145438-94-4,145438-95-5,145513-90-2,145513-91-3,145513-92-4,145513-93-5,2055118-14-2

(+/-)-(2S,3aS,7aS)-octahydroindole-2-carboxylic acid

(+/-)-(2R,3aS,7aS)-octahydroindole-2-carboxylic acid
80828-13-3,80875-98-5,82717-40-6,87679-20-7,87679-39-8,87679-51-4,87679-58-1,88547-85-7,88585-94-8,96844-78-9,108507-42-2,145438-94-4,145438-95-5,145513-90-2,145513-91-3,145513-92-4,145513-93-5,2055118-14-2

(+/-)-(2R,3aS,7aS)-octahydroindole-2-carboxylic acid

Conditions
Conditions Yield
With hydrogen; acetic acid; platinum(IV) oxide; at 60 ℃; for 24h;
70%

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