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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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A151275-1ml
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1ml |
5
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$9.90
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A151275-5ml
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5ml |
5
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$28.90
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A151275-25ml
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25ml |
4
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$91.90
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A151275-100ml
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100ml |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
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$328.90
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| 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. |
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 |
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| 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= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 25, 2022 | A151275 | |
| Certificate of Analysis | Jun 09, 2022 | A151275 | |
| Certificate of Analysis | Jun 09, 2022 | A151275 | |
| Certificate of Analysis | Jun 09, 2022 | A151275 | |
| Certificate of Analysis | Jun 09, 2022 | A151275 | |
| Certificate of Analysis | Jun 09, 2022 | A151275 | |
| Certificate of Analysis | Oct 08, 2021 | A151275 |
| 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 |
| 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). |