854371-84-9Relevant articles and documents
Biaryl sulfonamides and methods for using same
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Page/Page column 29, (2008/06/13)
The present invention relates to biaryl sulfonamides and their use as, for example, metalloproteinase inhibitors.
854371-84-9
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Basic information
- Product Name: 2-[4-(2-Chloro-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
- Synonyms:
- CAS NO:854371-84-9
- Molecular Formula:
- Molecular Weight: 344.646
- EINECS: N/A
- Product Categories: N/A
- Mol File: 854371-84-9.mol
- Article Data: 1
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 2-[4-(2-Chloro-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(CAS DataBase Reference)
- NIST Chemistry Reference: 2-[4-(2-Chloro-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(854371-84-9)
- EPA Substance Registry System: 2-[4-(2-Chloro-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane(854371-84-9)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 854371-84-9(Hazardous Substances Data)
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854371-84-9 Usage
Molecular structure
2-[4-(2-Chloro-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane is a boronic acid derivative that contains a dioxaborolane group.Usage
It is commonly used in the field of organic synthesis, particularly as a reagent for Suzuki-Miyaura cross-coupling reactions.Applications
It is often utilized in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals, due to its ability to efficiently form carbon-carbon bonds under mild reaction conditions.Stability
It has been shown to exhibit good stability and compatibility with a wide range of functional groups.Advantages
It is a valuable tool for researchers in the development of new chemical reactions and processes.Check Digit Verification of cas no
The CAS Registry Mumber 854371-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,3,7 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.Calculate Digit Verification of CAS Registry Number 854371-84:
(8*8)+(7*5)+(6*4)+(5*3)+(4*7)+(3*1)+(2*8)+(1*4)=189
189 % 10 = 9
So 854371-84-9 is a valid CAS Registry Number.
854371-84-9Upstream product
854371-84-9Downstream Products
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2-[4-(2-Chloro-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
