804559-38-4

Basic information

• Product Name: (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98%
• Synonyms: (R,R)-1,3-Bis-(4-broMobenzyl)-2-chlorooctahydro-2-(2Z)-crotyl-1H-1,3,2-benzodiazasilole;(3aR,7aR)-1,3-Bis[(4-bromophenyl)methyl]-2-(2Z)-2-buten-1-yl-2-chlorooctahydro-1H-1,3,2-benzodiazasilole;(1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98%
• CAS NO: 804559-38-4
• Molecular Formula: C₂₄H₂₉Br₂ClN₂Si
• Molecular Weight: 568.84696
• Mol File: 804559-38-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98%(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98%(804559-38-4)
• EPA Substance Registry System: (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98%(804559-38-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37
• Hazardous Substances Data: 804559-38-4(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98% is used as a reagent for the formation of carbon-silicon bonds. Its unique structure allows for the creation of new linkages between organic and silicon-based molecules, which is valuable in the synthesis of various functionalized organic compounds.
Used in Research Applications:
Due to its high purity and chiral nature, (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98% is utilized in research settings to explore the properties and reactions of chiral molecules. (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98% can be employed to study stereoselective reactions and to develop new methods for the synthesis of enantiomerically pure compounds.
Used in Pharmaceutical Industry:
(1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98% can be used as a building block or intermediate in the synthesis of pharmaceutical compounds. Its ability to form carbon-silicon bonds and its chiral properties make it a valuable component in the development of new drugs with specific biological activities.
Used in Material Science:
In the field of material science, (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98% may be employed to develop new materials with unique properties. (1R,2R)-(-)-[N,N'-Bis(4-bromobenzyl)-1,2-cyclohexanediamino][(2Z)-2-buten-1-yl]chlorosilane, min. 98%'s ability to form stable bonds with both organic and inorganic components can contribute to the creation of advanced materials for various applications, such as sensors, catalysts, or coatings.

Upstream product

• 18147-55-2 (Z)-crotyltrichlorosilane 
• 546084-44-0 (1R,2R)-N,N'-di(4'-bromobenzyl)-1,2-diaminocyclohexane 

Downstream Products

• 1292811-33-6 C₂₂H₃₈O₂Si 
• 157542-41-1 (2R,3R)-1-benzyloxy-3-methyl-4-penten-2-ol 
• 129170-74-7 (3R,4R)-4-methyl-1-phenylhex-5-en-3-ol? 
• 137819-50-2 (3R,4R)-1-(benzyloxy)-4-methylhex-5-en-3-ol 
• 1357163-01-9 (1E,4R,5R)-1-(2-methoxyphenyl)-5-methylhepta-1,6-dien-4-ol 
• 1357163-05-3 (1Z,4R,5R)-2-bromo-5-methyl-1-phenylhepta-1,6-dien-4-ol 
• 1357163-03-1 (1E,4R,5R)-5-methyl-1-(2-nitrophenyl)hepta-1,6-dien-4-ol 
• 1357162-96-9 (1E,4R,5R)-5-methyl-1-phenylhepta-1,6-dien-4-ol 
• 121155-52-0 (3R,4R)-4-cyclohexyl-3-methyl-1-buten-4-ol 
• 25201-44-9 (1S,2R)-2-methyl-1-phenylbut-3-en-1-ol 
• 25201-44-9 (1R,2S)-2-methyl-1-phenylbut-3-en-1-ol 
• 804559-44-2 (+)-(3R,4R)-1-[(4-methoxybenzyl)oxy]-4-methylhex-5-en-3-ol 
• 79298-54-7 (-)-(2S,3S)-1-Benzyloxy-3-methyl-4-penten-2-ol 
• 207503-57-9 (-)-(3S,4R)-4-methyl-1-phenylhex-5-en-3-ol 

Relevant articles and documents

Highly diastereo- and enantioselective reagents for aldehyde crotylation

(Chemical Equation Presented) Two new, crystalline solid, storable, and highly enantioselective reagents for aldehyde crotylation have been developed. Both (cis and trans) crotylsilane reagents are easily prepared in bulk, require trivial reaction conditi