124414-37-5

Basic information

• Product Name: 1,1-Binaphthalene-2,2-dithiol, (1R)-
• Synonyms: 1,1-Binaphthalene-2,2-dithiol, (1R)-;R-1,1'-binaphthalene]-2,2'-dithiol
• CAS NO: 124414-37-5
• Molecular Formula: C₂₀H₁₄S₂
• Molecular Weight: 318.46
• Mol File: 124414-37-5.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1-Binaphthalene-2,2-dithiol, (1R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-Binaphthalene-2,2-dithiol, (1R)-(124414-37-5)
• EPA Substance Registry System: 1,1-Binaphthalene-2,2-dithiol, (1R)-(124414-37-5)

Safety Data

• Hazardous Substances Data: 124414-37-5(Hazardous Substances Data)

Usage

Chiral compound

1,1-Binaphthalene-2,2-dithiol, (1R)is a chiral compound, meaning it has a specific arrangement of atoms in space that makes it different from its mirror image.

Member of the binaphthalene family

It is a member of the binaphthalene family, which are compounds with two naphthalene rings connected by a central sulfur atom.

Stereochemistry

The (1R)designation indicates the stereochemistry of the molecule, which refers to the spatial arrangement of atoms in the molecule.

Suitable for use in organic electronics

It has properties that make it suitable for use in organic electronics.

Building block for synthesis

It can be used as a building block for the synthesis of complex molecules.

Upstream product

• 147923-23-7 <1,1'-Binaphthalene>-2,2'-diyl S,S-bis(N,N-dimethylthiocarbamate) 
• 120577-40-4 C₂₉H₂₄O₅S₂ 
• 188-57-8 (R)-(-)-dinaphtho<2,1-c:1',2'-e><1,2>dithiin 
• 157367-47-0 pentanethioic acid S,S'-<(1,1'-binaphthalene)-2,2'-diyl> ester 
• 194-65-0 1,1'-binaphthothiophene 
• 602-09-5 1,1'-bi-2-naphthol 
• 120546-24-9 (+/-)-7,10-Dithiadinaphtho<2,1-d:1',2'-f>cyclooctene 7,7,10,10-tetraoxide 
• 121472-80-8 Dinaphtho<2,1-d:1',2'-g><1,4>dithiocine 
• 188-57-8 Dinaphtho<2,1-c:1',2'-e><1,2>dithiane 
• 124414-33-1 Dinaphtho<2,1-d:1',2'-f><1,4>dithiocane S-oxide 
• 124414-28-4 (2,2'-Dimethylthio)<1,1'-binaphthalene> 
• 124414-28-4 (2,2'-Dimethylthio) 
• 124414-32-0 (2-Methylsulfinyl-2'-methylthio)<1,1'-binaphthalene> 
• 124414-29-5 Dinaphtho<2,1-d:1',2'-g><1,4>dithiocane 

Downstream Products

• 126865-48-3 2-Benzoyldinaphtho<2,1-d:1',2'-f><1,3>dithiepine 
• 188-57-8 (R)-(-)-dinaphtho<2,1-c:1',2'-e><1,2>dithiin 
• 162825-40-3 (S)-4<(1''R,2''S,3''R,4''R)-1'',2'',3'',4'',5''-pentamethoxypentyl>-dinaphtho<2,1-d:1',2'-f><1,3>dithipin 
• 55441-99-1 (+)-<1,1'-binaphthalene>-2,2'-dithiol 
• 55441-99-1 (-)-<1,1'-binaphthalene>-2,2'-dithiol 
• 126865-50-7 2-(1-Phenyl-1-hydroxyethyl)dinaphtho<2,1-d:1',2'-f><1,3>dithiepine 
• 126865-51-8 2-Benzoylbinaphtho<2,1-d:1',2'-f><1,3>dithiepine S-oxide 
• 126865-52-9 2-(1-Phenyl-1-hydroxyethyl)dinaphtho<2,1-d:1',2'-f><1,3>dithiepine S-oxide 

Relevant articles and documents

A Chiral, Dendralenic C-H Acid

We report the synthesis of a chiral dendralenic C H acid, which contains three unsubstituted binaphthyl moieties. This motif and an achiral variant can be made from their corresponding bis(sulfone) precursors in one step. Despite the presence of the enantiopure binaphthyl backbone, the newly designed chiral C H acid showed only poor enantioselectivity in a Mukaiyama aldol reaction. First attempts toward the synthesis of 3,3'-hexasubstituted binaphthyl-based dendralenic acids are also reported.

Method for preparing substituted thiophenol and heterocyclic thiophenol by continuous flow reactor

The invention relates to a method for preparing substituted thiophenol and heterocyclic thiophenol by a continuous flow reactor. Phenol and phenol derivatives or heterocyclic phenol are taken as starting materials, and target compounds are prepared by four-step reactions of chlorination, esterification, rearrangement and hydrolysis, wherein the rearrangement reaction is conducted in the continuousflow reactor. According to the method, the reaction is guaranteed by a miniaturized heating device for high-temperature reaction and heat generated by the reaction, the conversion rate and the yieldhigher than those in the conventional reactor are obtained in the short residence time of tens of seconds, relevant side reactions are reduced, meanwhile, fluctuation of temperature and concentrationis avoided in the reaction process, temperature run-away and overheat are avoided, and the reaction process is safe and controllable.

Practical synthetic approach to chiral sulfonimides (CSIs) - Chiral bronsted acids for organocatalysis

A general approach to the synthesis of optically pure 3,3'diaryl chiral sulfonimides (CSIs) from racemic BINOL has been developed. ortho-Lithiation is directed by the sulfonyl groups, and the resulting dihalides serve as the common precursors for the aryl-substituted CSIs.