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(Bromodifluoromethyl)trimethylsilane - >98.0%(GC), high purity , CAS No.115262-01-6

    Grade & Purity:
  • ≥98%(GC)
In stock
Item Number
B152721
Grouped product items
SKU Size
Availability
Price Qty
B152721-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$75.90
B152721-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$226.90
B152721-25g
25g
2
$1,017.90

Basic Description

Synonyms [bromo(difluoro)methyl](trimethyl)silane | Bromodifluoro(trimethylsilyl)methane | SY047583 | C4H9BrF2Si | MS-20546 | B4325 | (Bromodifluoromethyl)trimethylsilane, 98% | [Bromo(difluoro)methyl]trimethylsilane | [bromo(difluoro)methyl]-trimethylsilane | A85
Specifications & Purity ≥98%(GC)
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

(Bromodifluoromethyl)trimethylsilane (TMSCF2Br) is commonly used as a source to generate dilfluorocarbene. TMSCF3 (Ruppert-Prakash reagent) and BBr3undergoes fast halogen-exchange reaction to form MSCF2Br.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organohalogen compounds
Class Alkyl halides
Subclass Halomethanes
Intermediate Tree Nodes Not available
Direct Parent Trihalomethanes
Alternative Parents Organic metalloid salts  Organofluorides  Organobromides  Hydrocarbon derivatives  Alkylsilanes  Alkyl fluorides  Alkyl bromides  
Molecular Framework Aliphatic acyclic compounds
Substituents Trihalomethane - Organic metalloid salt - Hydrocarbon derivative - Organosilicon compound - Alkylsilane - Organofluoride - Organobromide - Organic metalloid moeity - Alkyl fluoride - Alkyl bromide - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as trihalomethanes. These are organic compounds in which exactly three of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
External Descriptors Not available

Names and Identifiers

IUPAC Name [bromo(difluoro)methyl]-trimethylsilane
INCHI InChI=1S/C4H9BrF2Si/c1-8(2,3)4(5,6)7/h1-3H3
InChIKey WDZVWBWAUSUTTO-UHFFFAOYSA-N
Smiles C[Si](C)(C)C(F)(F)Br
Isomeric SMILES C[Si](C)(C)C(F)(F)Br
Molecular Weight 203.1
Reaxy-Rn 3535353
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3535353&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot Number Certificate Type Date Item
B2216100 Certificate of Analysis Dec 25, 2023 B152721
C2009047 Certificate of Analysis Jan 21, 2022 B152721
B2216101 Certificate of Analysis Jan 10, 2022 B152721

Chemical and Physical Properties

Sensitivity Air & light & heat & Moisture sensitive
Refractive Index 1.407
Flash Point(°C) 17 °C
Boil Point(°C) 108°C(lit.)
Molecular Weight 203.100 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 1
Exact Mass 201.963 Da
Monoisotopic Mass 201.963 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 86.500
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Zhenrui Li, Haifeng Zuo, Minglei Su, Zhenbing Sun, Jianfeng Ma, Xing’e Liu, Pengyi Zhang.  (2025)  Enhancing the adsorption capacity of lignin-based super activated carbon for trace toluene under highly humid conditions through [2 + 1] cycloaddition reactions.  CHEMICAL ENGINEERING JOURNAL,  509  (161421). 

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