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1,2,4,3,5-Dithiazadiborolidine, 3,5-dibromo-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94397-75-8

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94397-75-8 Usage

Structure

Contains boron and nitrogen atoms, diborane(4) reagent with a boron-boron single bond and two bridging nitrogen atoms

Functional groups

Two bromine atoms and a phenyl group attached to the boron atoms

Organic synthesis

Used as a reagent for a variety of reactions

Catalysis

Facilitates carbon-carbon and carbon-heteroatom bond-forming reactions

Materials science

Studied for potential applications in the development of new functional materials

Reactivity

Active in various chemical reactions due to its unique structure and functional groups

Stability

Relatively stable under controlled conditions, but may react with other chemicals or reagents

Solubility

Soluble in organic solvents, such as dichloromethane or tetrahydrofuran

Safety

Handle with care, as it may be toxic or hazardous depending on its concentration and exposure

Storage

Store in a cool, dry, and well-ventilated area, away from incompatible substances

Purity

Typically synthesized with high purity for use in research and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 94397-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94397-75:
(7*9)+(6*4)+(5*3)+(4*9)+(3*7)+(2*7)+(1*5)=178
178 % 10 = 8
So 94397-75-8 is a valid CAS Registry Number.

94397-75-8Relevant academic research and scientific papers

1,4-Dithia-2,6-diaza-3,5-diborinanes: A Novel B-N-S-Ringsystem

Habben, Carl,Meller, Anton

, p. 1022 - 1026 (2007/10/02)

The novel 1,4-dithia-2,6-diaza-3,5-diborinane ring system results from the reaction of 3,5-dialkyl- (or di-sec.amino-) substituted 1,2,4-trithia-3,5-diborolanes with 1,3-disubstituted sulfurdiimides by replacement of the disulfane bridge.Upon treatment with azomethines, 3,5-dibromo-1,2,4-trithia-3,5-diborolane gives 3,5-dibromo-1,2-dithia-4-aza-5-diborolidines by substitution of the sulfur atom in position 4. 1H, 11B, 13C, 29Si NMR and mass spectra are reported and discussed. - Keywords: 1,4-Dithia-2,6-diaza-3,5-diborinanes, 1,2-Dithia-4-aza-3,5-diborolidines, 1,2,4-Trithia-3,5-diborolanes, Sulfurdiimides, Azomethines

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