144069-67-0

Basic information

• Product Name: BOC-(2S)-INDOLINE CARBOXYLIC ACID
• Synonyms: BOC-(2S)-INDOLINE CARBOXYLIC ACID;BOC-IDC-OH;BOC-L-INDOLINE-2-CARBOXYLIC ACID;BOC-L-IDC-OH;RARECHEM EM WB 0142;(S)2,3-DIHYDRO-INDOLE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER;(S)-N-ALPHA-TERT-BUTYLOXYCARBONYL-2-INDOLINECARBOXYLIC ACID;(R)-N-alpha-t-Butyloxycarbonyl-2-indolinecarboxylic acid
• CAS NO: 144069-67-0
• Molecular Formula: C₁₄H₁₇NO₄
• Molecular Weight: 263.29
• Product Categories: Amino Acids
• Mol File: 144069-67-0.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Storage Temp.: Store at 0°C
• CAS DataBase Reference: BOC-(2S)-INDOLINE CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-(2S)-INDOLINE CARBOXYLIC ACID(144069-67-0)
• EPA Substance Registry System: BOC-(2S)-INDOLINE CARBOXYLIC ACID(144069-67-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 144069-67-0(Hazardous Substances Data)

Usage

Chemical Properties

Off-white solid

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 79815-20-6 (S)-indoline-2-carboxylic acid 
• 186704-03-0 methyl (+/-)-1-t-butoxycarbonyl-indoline-2-carboxylate 
• 1202-04-6 indole-2-carboxylic acid methyl ester 
• 3770-50-1 2-carbethoxyindole 
• 101137-66-0 methyl2-<(E)-phenylhydrazono>propionate 
• 59040-84-5 indoline-2-carboxylic acid methyl ester 
• 62-53-3 aniline 
• 163229-48-9 1-(1,1-dimethylethyl)-1H-indole-1,2-dicarboxylic acid 2-methyl ester 
• 13732-33-7 ethyl α-(E-phenylhydrazono)propionate 

Downstream Products

• 176714-25-3 (S)-2-{(2S,4R)-2-[(2S,3aS,6aS)-2-(Benzyl-methyl-carbamoyl)-hexahydro-cyclopenta[b]pyrrole-1-carbonyl]-4-hydroxy-pyrrolidine-1-carbonyl}-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester 
• 176714-26-4 (S)-2-{(2S,4R)-2-[(S)-2-(Benzyl-methyl-carbamoyl)-2,3-dihydro-indole-1-carbonyl]-4-hydroxy-pyrrolidine-1-carbonyl}-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester 
• 176714-24-2 (S)-2-{(2S,4R)-2-[(S)-3-(Benzyl-methyl-carbamoyl)-3,4-dihydro-1H-isoquinoline-2-carbonyl]-4-hydroxy-pyrrolidine-1-carbonyl}-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester 
• 678988-10-8 (S)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2,3-dihydroindole-2-carboxamide 
• 338463-31-3 (S)-2-((4-(methoxycarbonylpropyl)phenyl)aminocarbonyl)indoline 
• 926893-38-1 (S)-N-(2,6-dimethylphenyl)-indoline-2-carboxamide 
• 950196-01-7 C₂₀H₂₁N₃O₇S 
• 950196-02-8 C₂₀H₂₀N₂O₆ 
• 950196-03-9 C₂₁H₂₄N₂O₅S 
• 950196-04-0 C₂₉H₄₀N₂O₅S 
• 886447-93-4 ethyl [4-[1-[3-methoxy-4-[N'-(2-methylphenyl)ureido]phenylacetyl]-2,3-dihydro-1H-(2S)-indolylcarbonyl]-1-piperazinyl]acetate 
• 141410-06-2 (S)-indoline-2-carboxylic acid methyl ester 
• 678988-11-9 (S)-N,N-dibenzyl-2,3-dihydro-1H-indole-2-carboxamide 

Relevant articles and documents

COSMETIC USES AND METHODS FOR INDOLINE GRANZYME B INHIBITOR COMPOSITIONS

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.

New P-stereogenic triaminophosphines and their derivatives: Synthesis, structure, conformational study, and application as chiral ligands

The synthesis, structural, and conformational studies of new P-chiral triaminophosphines, which feature an indolidine and a 1,2,3,4- tetrahydroquinolidine pattern, respectively, are reported. These compounds can feature very different 3D-structures, although they both could be seen a priori as close derivatives of the previously reported 3-phenyl-1,3-diaza-2- phosphabicyclo[3.3.0]octane. The consequences for the use of such compounds and their derivatives in asymmetric metal-catalysis are discussed on the basis of preliminary results in asymmetric cobalt-catalyzed [6+2] cycloaddition.

Application of novel sulfonamides in enantioselective organocatalyzed cyclopropanation

Three novel aryl sulfonamides derived from (2S)-indoline-2-carboxylic acid have been obtained and used as organocatalysts. The catalysts incorporate diverse functionality on the phenyl ring, enabling steric, and electronic fine tuning of the catalysts. Th