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Allyltrimethoxysilane - >97.0%(GC), high purity , CAS No.2551-83-9

    Grade & Purity:
  • ≥97%(GC)
In stock
Item Number
A151275
Grouped product items
SKU Size
Availability
Price Qty
A151275-1ml
1ml
5
$9.90
A151275-5ml
5ml
5
$28.90
A151275-25ml
25ml
4
$91.90
A151275-100ml
100ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$328.90

Basic Description

Synonyms A901416 | Allyltrimethoxysilane, 95% | SCHEMBL93295 | J-016033 | FT-0694825 | FS-4958 | LFRDHGNFBLIJIY-UHFFFAOYSA-N | Silane, trimethoxy-2-propenyl- | MFCD00053865 | AKOS008901195 | Silane, allyltrimethoxy- | Allyltrimethoxysilane, >=98%, deposition grade
Specifications & Purity ≥97%(GC)
Storage Temp Argon charged
Shipped In Normal
Product Description

Allyltrimethoxysilane is an allylating reagent that can be used for the allylation of carbonyl compounds such as aldehydes, ketones, and imines. Homoallylic alcohols and amines are obtained via the C-C bond forming reaction.It can also be used to synthesize homoallylic α-branched amines from aromatic and aliphatic aldehyde hydrazones, and ketone hydrazones.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organometallic compounds
Class Organometalloid compounds
Subclass Organosilicon compounds
Intermediate Tree Nodes Alkoxysilanes
Direct Parent Trialkoxysilanes
Alternative Parents Silyl ethers  Organoheterosilanes  Organic metalloid salts  Organooxygen compounds  Hydrocarbon derivatives  
Molecular Framework Aliphatic acyclic compounds
Substituents Trialkoxysilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl group).
External Descriptors Not available

Names and Identifiers

Pubchem Sid 488185156
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488185156
IUPAC Name trimethoxy(prop-2-enyl)silane
INCHI InChI=1S/C6H14O3Si/c1-5-6-10(7-2,8-3)9-4/h5H,1,6H2,2-4H3
InChIKey LFRDHGNFBLIJIY-UHFFFAOYSA-N
Smiles CO[Si](CC=C)(OC)OC
Isomeric SMILES CO[Si](CC=C)(OC)OC
WGK Germany 3
UN Number 1993
Packing Group III
Molecular Weight 162.26
Beilstein 2350750
Reaxy-Rn 2350745
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2350745&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.

7 results found

Lot Number Certificate Type Date Item
G2215019 Certificate of Analysis Jul 25, 2022 A151275
C2306927 Certificate of Analysis Jun 09, 2022 A151275
H2217065 Certificate of Analysis Jun 09, 2022 A151275
H2217066 Certificate of Analysis Jun 09, 2022 A151275
C2306928 Certificate of Analysis Jun 09, 2022 A151275
H2217067 Certificate of Analysis Jun 09, 2022 A151275
C2306926 Certificate of Analysis Oct 08, 2021 A151275

Chemical and Physical Properties

Sensitivity Moisture sensitive
Refractive Index 1.405
Flash Point(°F) 114.8 °F
Flash Point(°C) 31°C
Boil Point(°C) 136°C
Molecular Weight 162.260 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 5
Exact Mass 162.071 Da
Monoisotopic Mass 162.071 Da
Topological Polar Surface Area 27.700 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 92.900
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. Bo Wang, Jianhua Sha, Shuaishuai Chen, Weiyan Yin, Yude Li, Qinyan Yue, Haiyan Yu, Shiping Xu.  (2023)  Enhanced adsorption-photocatalysis synergy and stability of polypropylene photocatalytic floating ball benefitted from click chemistry connection.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,  443  (114883). 

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