(4-bromobut-1-enyl)cyclopropane is a halogenated cyclopropane derivative, consisting of a cyclopropane ring with a 4-bromobut-1-enyl group attached to it. The cyclopropane ring is highly reactive and strained, making it a valuable building block for the synthesis of various organic compounds. The presence of the bromine atom in the molecule adds additional properties and reactivity, making it useful for a wide range of applications in organic synthesis and chemical research.
1489-73-2
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Basic information
- Product Name: (4-bromobut-1-enyl)cyclopropane
- Synonyms: (4-bromobut-1-enyl)cyclopropane;(4-Bromo-1-butenyl)cyclopropane
- CAS NO:1489-73-2
- Molecular Formula: C7H11Br
- Molecular Weight: 175.06624
- EINECS: 216-073-9
- Product Categories: N/A
- Mol File: 1489-73-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 184.5°Cat760mmHg
- Flash Point: 61.9°C
- Appearance: /
- Density: 1.473g/cm3
- Vapor Pressure: 0.998mmHg at 25°C
- Refractive Index: 1.623
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (4-bromobut-1-enyl)cyclopropane(CAS DataBase Reference)
- NIST Chemistry Reference: (4-bromobut-1-enyl)cyclopropane(1489-73-2)
- EPA Substance Registry System: (4-bromobut-1-enyl)cyclopropane(1489-73-2)
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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: 1489-73-2(Hazardous Substances Data)
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1489-73-2 Usage
Uses
Used in Organic Synthesis:(4-bromobut-1-enyl)cyclopropane is used as a building block for the synthesis of various organic compounds due to its highly reactive and strained cyclopropane ring. The presence of the bromine atom further enhances its reactivity, making it a versatile compound for creating a wide range of organic molecules.
Used in Chemical Research:
(4-bromobut-1-enyl)cyclopropane is used as a research compound for studying the properties and reactivity of halogenated cyclopropane derivatives. Its unique structure and reactivity make it an interesting subject for chemical research, allowing scientists to explore new reactions and applications in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1489-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.Calculate Digit Verification of CAS Registry Number 1489-73:
(6*1)+(5*4)+(4*8)+(3*9)+(2*7)+(1*3)=102
102 % 10 = 2
So 1489-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H11Br/c8-6-2-1-3-7-4-5-7/h1,3,7H,2,4-6H2/b3-1+
1489-73-2Upstream product
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(4-bromobut-1-enyl)cyclopropane
