1025-09-8

Basic information

• Product Name: Silane, methyl-1-naphthalenylphenyl-, (S)-
• CAS NO: 1025-09-8
• Molecular Formula: C17H16Si
• Molecular Weight: 248.4
• Mol File: 1025-09-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Silane, methyl-1-naphthalenylphenyl-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, methyl-1-naphthalenylphenyl-, (S)-(1025-09-8)
• EPA Substance Registry System: Silane, methyl-1-naphthalenylphenyl-, (S)-(1025-09-8)

Safety Data

• Hazardous Substances Data: 1025-09-8(Hazardous Substances Data)

Upstream product

• 3027-21-2 dimethoxy(methyl)phenylsilane 
• 703-55-9 1-naphthylmagnesiumbromide 
• 917-64-6 methyl magnesium iodide 
• 111949-31-6 (5S,6S)-2-ethyl-5,6-dimethoxy-2-phenyl-1,3-dioxa-2-silacycloheptane 
• 111949-29-2 (5S,6S)-5,6-dimethoxy-2-methyl-2-(1-naphthyl)-1,3-dioxa-2-silacycloheptane 
• 100-58-3 phenylmagnesium bromide 
• 3553-88-6 (-)-1-Naphthylphenylmethylmethoxysilan 
• 13132-41-7 (S)-Fluoro-methyl-naphthalen-1-yl-phenyl-silane 
• 56-23-5 tetrachloromethane 
• 1025-08-7 (R)-methyl(1-naphthyl)phenylsilane 
• 7782-50-5 chlorine 
• 17998-62-8 dichloro-α-naphthylmethylsilane 
• 1125-27-5 dichloro(ethyl)phenylsilane 
• 90-14-2 1-Iodonaphthalene 

Downstream Products

• 18720-42-8 fluoromethylphenyl-silane 
• 36260-50-1 α-naphthylphenylmethylfluorosilane 
• 960-82-7 (+)-methylphenylnaphthylchlorosilane 
• 3553-88-6 (-)-1-Naphthylphenylmethylmethoxysilan 
• 76226-95-4 (+)α-naphthylphenylmethyloctylsilane 
• 119908-54-2 (S)-(4,4-Dimethyl-pent-1-ynyl)-methyl-naphthalen-1-yl-phenyl-silane 
• 119908-52-0 (R)-(4,4-Dimethyl-penta-1,2-dienyl)-methyl-naphthalen-1-yl-phenyl-silane 
• 50881-11-3 (R)-Methyl-naphthalen-1-yl-phenyl-propa-1,2-dienyl-silane 
• 13132-42-8 (R)-(+)-chloromethyl(1-naphthyl)phenylsilane 

Relevant articles and documents

Synthesis of optically active tertiary silanes via Pd-catalyzed enantioselective arylation of secondary silanes

We herein describe the development of an efficient enantioselective catalytic system that promotes the arylation of secondary silanes. Our method involves treatment of secondary silanes and aryl iodides with a Pd 2(dba)3-asymmetric p

A stereoselective approach to optically active bifunctional 1,3-dimethyl-1,3-diphenyldisiloxanes

(Matrix presented) Functionalized disiloxanes have attracted much attention as versatile synthetic intermediates in the preparation of disiloxane-containing polymers. In this report, a highly stereoselective (98% inversion) halogenating cleavage reaction of the silicon-naphthyl bond to obtain optically active (S,S)-1,3-dimethyl-1,3-diphenyldisiloxanediol ((S,S):(R,S):(R,R) = 86:14:0) was demonstrated.