119807-82-8

Basic information

• Product Name: (R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER
• Synonyms: (R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER
• CAS NO: 119807-82-8
• Molecular Formula: C15H14O4
• Molecular Weight: 258.27
• Mol File: 119807-82-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER(119807-82-8)
• EPA Substance Registry System: (R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER(119807-82-8)

Safety Data

• Hazardous Substances Data: 119807-82-8(Hazardous Substances Data)

Usage

General Description

"(R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER" is a chemical compound with the molecular formula C17H18O4. It is a methyl ester of (R)-2-(1-naphthylmethyl)succinic acid and is commonly used as a chiral building block in organic synthesis. (R)-2-(1-NAPHTHYLMETHYL)-SUCCINIC ACID-1-METHYL ESTER has potential applications in pharmaceuticals, agrochemicals, and materials science. It is a white solid that is soluble in organic solvents and has a characteristic sweet odor. It is important to handle this chemical with care as it may have hazardous effects if not properly managed.

Upstream product

• 106-65-0 Dimethyl succinate 
• 66-77-3 1-naphthaldehyde 
• 17917-18-9 (E)-2-(1-naphthylmethylene)succinic acid 1-methyl ester 
• 130561-76-1 3-(methoxycarbonyl)-4-(1-naphthyl)-3-butenoic acid 

Relevant articles and documents

Modular 1,1′-Ferrocenediyl-cored P-Stereogenic Diphosphines: ′′JDayPhos′′ Series and its Use in Rhodium(I)-Catalyzed Hydrogenation

A novel ferrocene-based P-stereogenic diphospine ligand series dubbed JDayPhos was developed, which rhodium(I) complexes of some of its members exhibited excellent enantioselectivity (up to >99% ee) and high activity in asymmetric hydrogenation of β-unsubstituted or -substituted itaconates and α-methylene-γ-oxo-carboxylates. (Figure presented.).

Practical access to 2-alkylsuccinates through asymmetric catalytic hydrogenation of Stobbe-derived itaconates

Enantiomerically pure 2-alkylsuccinates are obtained on a 500-g scale after hydrogenation with the cationic rhodium complexes with tetraalkyl-substituted 1,2-bis(phospholanyl)ethane or -benzene ligands [R'-DuPHOS; Eq. (a)]. The catalysts allow smooth hydr

Non-peptidyl beta-succinamidoacyl aminodiols as anti-hypertensive agents

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