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(2S)-2-(naphthalen-2-yloxy)butanoic acid is a chiral organic compound with the molecular formula C14H14O3. It is a derivative of butanoic acid, featuring a naphthalene moiety attached to the second carbon atom through an ether linkage. (2S)-2-(naphthalen-2-yloxy)butanoic acid is characterized by its specific stereochemistry, with the "2S" notation indicating that the hydroxyl group is on the left side when looking at the molecule from the perspective of the carbon-carbon single bond. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural properties. The compound's naphthalene ring provides it with a distinct aromatic character, which can influence its reactivity and interactions with other molecules.

7668-56-6

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7668-56-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7668-56-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,6 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7668-56:
(6*7)+(5*6)+(4*6)+(3*8)+(2*5)+(1*6)=136
136 % 10 = 6
So 7668-56-6 is a valid CAS Registry Number.

7668-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(naphthalen-2-yloxy)butyric acid

1.2 Other means of identification

Product number -
Other names (S)-2-(2-naphthyloxy)butanoic acid

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:7668-56-6 SDS

7668-56-6Downstream Products

7668-56-6Relevant academic research and scientific papers

Enantioselective hydrogenation of α-aryloxy and α-alkoxy α,β-unsaturated carboxylic acids catalyzed by chiral spiro iridium/phosphino-oxazoline complexes

Li, Shen,Zhu, Shou-Fei,Xie, Jian-Hua,Song, Song,Zhang, Can-Ming,Zhou, Qi-Lin

supporting information; experimental part, p. 1172 - 1179 (2010/04/01)

The iridium-catalyzed highly enantioselective hydrogenation of α-aryloxy and α-alkoxy-substituted α,β-unsaturated carboxylic acids was developed. By using chiral spiro phosphino-oxazoline ligands, the hydrogenation proceeded smoothly to produce various α-aryloxy- and α-alkoxy-substituted carboxylic acids with extremely high enantioselectivities (ee up to 99.8%) and reactivities (TON up to 10 000) under mild conditions. The hydrogenation of R-benzyloxy-substituted α,β-unsaturated acids provided an efficient alternative for the synthesis of chiral R-hydroxy acids after an easy deprotection. A mechanism involving a catalytic cycle between IrI and IrIII was proposed on the basis of the coordination model of the unsaturated acids with the iridium metal center. The rationality of the catalytic cycle, with an olefin dihydride complex as the key intermediate, was supported by the deuterium-labeling studies. The X-ray diffraction analysis of the single crystal of catalyst revealed that the rigid and sterically hindered chiral environment created by the spiro phosphino-oxazoline ligands is the essential factor that permits the catalyst to obtain excellent chiral discrimination. A chiral induction model was suggested on the basis of the catalyst structure and the product configuration.

Asymmetric hydrogenation of α,β-unsaturated carboxylic acids catalyzed by ruthenium(II) complexes of spirobifluorene diphosphine (SFDP) ligands

Cheng, Xu,Xie, Jian-Hua,Li, Sheng,Zhou, Qi-Lin

, p. 1271 - 1276 (2007/10/03)

The ruthenium diacetate complexes ligated by chiral spirobifluorene diphosphines (SFDP) were very effective catalysts for the asymmetric hydrogenation of tiglic acid derivatives and α-methylcinnamic acid derivatives with high activities and excellent enantioselectivities (up to 98% ee). The α-aryloxybutenoic acids can also be hydrogenated by these catalysts to provide the corresponding saturated α-aryloxybutanoic acids in high yields (89-93%) and enantioselectivities (up to 95% ee). In this reaction, the SFDP ligand with para-methyl groups on the P-phenyl rings gave the best results.

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