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(S)-Indoline-2-carboxylic acid ethyl ester, with the molecular formula C11H13NO2, is a derivative of the heterocyclic compound indoline, featuring a six-membered ring with nitrogen. This colorless to pale yellow liquid, characterized by a distinctive odor, is soluble in most organic solvents and has a broad spectrum of applications in organic synthesis and chemical research.

82923-81-7

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82923-81-7 Usage

Uses

Used in Pharmaceutical Industry:
(S)-Indoline-2-carboxylic acid ethyl ester is utilized as a building block for the synthesis of various drugs and pharmaceuticals, playing a crucial role in the development of new medicinal compounds.
Used in Research and Development:
In the realm of scientific research, (S)-Indoline-2-carboxylic acid ethyl ester serves as a key component in the exploration and creation of new chemical entities, contributing to the advancement of chemical knowledge and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 82923-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,2 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82923-81:
(7*8)+(6*2)+(5*9)+(4*2)+(3*3)+(2*8)+(1*1)=147
147 % 10 = 7
So 82923-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO2/c1-2-14-11(13)10-7-8-5-3-4-6-9(8)12-10/h3-6,10,12H,2,7H2,1H3/t10-/m0/s1

82923-81-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2S)-2,3-dihydro-1H-indole-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl (S)-2-indoline carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82923-81-7 SDS

82923-81-7Relevant academic research and scientific papers

COSMETIC USES AND METHODS FOR INDOLINE GRANZYME B INHIBITOR COMPOSITIONS

-

Page/Page column 71; 72, (2014/10/15)

Cosmetic uses and methods for indoline granzyme B inhibitor compounds in compositions with a cosmetically acceptable carrier. Uses and methods for treating, reducing or inhibiting the appearance of ageing in the skin are provided. Also provided are compositions and formulation for cosmetic uses and methods of maintaining a youthful appearance, reducing an appearance of ageing, inhibiting an appearance of ageing, reducing a rate of an appearance of ageing, reducing a skin inelasticity, reducing a rate of increasing skin inelasticity, maintaining a skin elasticity, and increasing the density of hair follicles of a skin of a subjecl. The uses and methods comprise applying/administering an indoline granzyme B inhibitor to a skin, or a portion of a skin of the subject.

Asymmetric 1,3-dipolar cycloaddition of nitrile oxides to new chiral acrylamides derived from (S)-indoline-2-carboxylic acid

Kim,Kim,Park

, p. 6063 - 6066 (2007/10/02)

Asymmetric 1,3-dipolar cycloaddition of nitrile oxides to new chiral acrylamides (3a-c) is reported to give the chiral Δ2-isoxazolines with the high diastereoselectivity (up to 95:5).

N-ACYL-gamma-GLUTAMYL IMINO AND AMINO ACIDS AND ESTERS

-

, (2008/06/13)

Compounds of the formula STR1 wherein X is various imino or amino acids or esters are disclosed. These compounds possess angiotensin converting enzyme inhibition activity and depending upon the definition of X also possess enkephalinase inhibition activit

1-mercaptoalkanoylindoline-2-carboxylic acids

-

, (2008/06/13)

1-Mercaptoalkanoylindoline-2-carboxylic acids, e.g., those of the formula STR1 and functional derivatives thereof, are antihypertensive and cardioactive agents.

1-Carboxyalkanoylindoline-2-carboxylic acids

-

, (2008/06/13)

1-Carboxy-(alkanoyl or aralkanoyl)-indoline-2-carboxylic acids, e.g., those of the formula STR1 R=H, alkyl, alkoxy, halogeno or CF3 ; R'=H or R-phenyl; m=0 or 1; p,q=0 to 2; and derivatives thereof, are antihypertensive and cardioactive agents.

1-CARBOXYALKANOYLINDOLINE-2-CARBOXYLIC ACIDS

-

, (2008/06/13)

1-Carboxy-(alkanoyl or aralkanoyl)-indoline-2-carboxylic acids, e.g., those of the formula STR1 R=H, alkyl, alkoxy, halogeno or CF. sub.3 ; R'=H or R-phenyl;m=0 or 1;p, q=0 to 2; and functional derivatives thereof, are antihypertensive a

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