[S,(+)]-1-Bromo-2,3-dimethylbutane is an organic compound with a specific stereochemistry, characterized by the presence of a bromine atom attached to a chiral carbon in the S configuration and a positive optical rotation. It is a versatile reagent in organic synthesis due to its unique structural features and reactivity.
15164-29-1
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Basic information
- Product Name: [S,(+)]-1-Bromo-2,3-dimethylbutane
- Synonyms: [S,(+)]-1-Bromo-2,3-dimethylbutane
- CAS NO:15164-29-1
- Molecular Formula: C6H13Br
- Molecular Weight: 165.07142
- EINECS: N/A
- Product Categories: Aliphatics, Miscellaneous Reagents
- Mol File: 15164-29-1.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: Chloroform, DCM, DMSO, Ethyl Acetate
- CAS DataBase Reference: [S,(+)]-1-Bromo-2,3-dimethylbutane(CAS DataBase Reference)
- NIST Chemistry Reference: [S,(+)]-1-Bromo-2,3-dimethylbutane(15164-29-1)
- EPA Substance Registry System: [S,(+)]-1-Bromo-2,3-dimethylbutane(15164-29-1)
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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: 15164-29-1(Hazardous Substances Data)
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15164-29-1 Usage
Uses
Used in Pharmaceutical Industry:[S,(+)]-1-Bromo-2,3-dimethylbutane is used as a synthetic reagent for the production of Campesterol (C155360), a phytosterol. Campesterol is known to inhibit the intestinal absorption of cholesterol, which can be beneficial in managing and treating conditions related to high cholesterol levels.
Used in Chemical Synthesis:
[S,(+)]-1-Bromo-2,3-dimethylbutane is used as a chiral building block in the synthesis of various organic compounds, particularly those requiring a specific stereochemistry. Its unique structure allows for selective reactions and the formation of complex molecules with desired properties.
Used in Research and Development:
In the field of research and development, [S,(+)]-1-Bromo-2,3-dimethylbutane serves as a valuable compound for studying the effects of stereochemistry on the properties and reactivity of molecules. It can be used to explore the relationship between molecular structure and biological activity, which is crucial in the design of new drugs and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 15164-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.Calculate Digit Verification of CAS Registry Number 15164-29:
(7*1)+(6*5)+(5*1)+(4*6)+(3*4)+(2*2)+(1*9)=91
91 % 10 = 1
So 15164-29-1 is a valid CAS Registry Number.
15164-29-1Upstream product
15164-29-1Downstream Products
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[S,(+)]-1-Bromo-2,3-dimethylbutane
