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Allyltrimethylsilane - 98%, high purity , CAS No.762-72-1

  • ≥98%
Item Number
A107288
Grouped product items
SKUSizeAvailabilityPrice Qty
A107288-5ml
5ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$16.90
A107288-10ml
10ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$24.90
A107288-25ml
25ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$47.90
A107288-50ml
50ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$85.90
A107288-100ml
100ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$153.90
A107288-250ml
250ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$275.90
A107288-500ml
500ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$495.90

Discover Allyltrimethylsilane by Aladdin Scientific in 98% for only $16.90. Available - in Ligands at Aladdin Scientific. Tags: Element classified compounds, Silicon compound.

Basic Description

SynonymsAllyltrimethylsilane|762-72-1|Silane, trimethyl-2-propenyl-|Trimethylallylsilane|3-(Trimethylsilyl)propene|trimethyl(prop-2-enyl)silane|Silane, allyltrimethyl-|allyl-trimethyl-silane|MFCD00008635|3-(Trimethylsilyl)-1-propene|trimethyl(prop-2-en-1-yl)silan
Specifications & Purity98%
Storage TempStore at 2-8°C
Shipped InWet ice

Names and Identifiers

IUPAC Name trimethyl(prop-2-enyl)silane
INCHI InChI=1S/C6H14Si/c1-5-6-7(2,3)4/h5H,1,6H2,2-4H3
InChi Key HYWCXWRMUZYRPH-UHFFFAOYSA-N
Canonical SMILES C[Si](C)(C)CC=C
Isomeric SMILES C[Si](C)(C)CC=C
WGK Germany 3
PubChem CID 69808
UN Number 1993
Molecular Weight 114.26
Beilstein 906755
Reaxy-Rn 906755

Certificates

Certificate of Analysis(COA)

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15 results found

Lot NumberCertificate TypeDateItem
F2404062Certificate of AnalysisJun 21, 2024 A107288
I2209127Certificate of AnalysisJun 12, 2024 A107288
I2209132Certificate of AnalysisJun 12, 2024 A107288
I2209133Certificate of AnalysisJun 12, 2024 A107288
I2209285Certificate of AnalysisJun 12, 2024 A107288
I2209288Certificate of AnalysisJun 12, 2024 A107288
I2209289Certificate of AnalysisJun 12, 2024 A107288
I2209292Certificate of AnalysisJun 12, 2024 A107288
F1807030Certificate of AnalysisNov 08, 2023 A107288
K2105467Certificate of AnalysisAug 04, 2023 A107288
H2113032Certificate of AnalysisMay 11, 2023 A107288
I1817149Certificate of AnalysisJun 24, 2022 A107288
I1812115Certificate of AnalysisMay 05, 2022 A107288
G1817063Certificate of AnalysisFeb 16, 2022 A107288
F1807001Certificate of AnalysisJan 11, 2022 A107288

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Chemical and Physical Properties

SensitivityMoisture Sensitive
Refractive Index1.407
Flash Point(°F)60.8 °F
Flash Point(°C)45 °F
Boil Point(°C)84-88°C

Safety and Hazards(GHS)

Pictogram(s) GHS07,   GHS02
Signal Danger
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

H225:Highly Flammable liquid and vapor

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P370+P378:In case of fire: Use ... to extinguish.

P210:Keep away from heat, hot surface, sparks, open flames and other ignition sources. - No smoking.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P233:Keep container tightly closed.

P240:Ground/bond container and receiving equipment.

P264:Wash hands [and …] thoroughly after handling.

P403+P235:Store in a well-ventilated place. Keep cool.

P303+P361+P353:IF ON SKIN (or hair): Take off Immediately all contaminated clothing. Rinse SKIN with water [or shower].

P271:Use only outdoors or in a well-ventilated area.

P241:Use explosion-proof [electrical/ventilating/lighting/.../] equipment.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P242:Use only non-sparking tools.

P243:Take precautionary measures against static discharge.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

WGK Germany 3
Reaxy-Rn 906755

Related Documents

References

1. J S Yadav,B V Reddy,L Chandraiah,K S Reddy.  (2001-07-04)  LiBF4-mediated C-glycosylation of glycals with allyltrimethylsilane: a facile synthesis of allyl C-glycosylic compounds..  Carbohydrate research,  332  ((2)): (221-224).  [PMID:11434381]
2. Satoru Tamura,Hiroshi Abe,Akira Matsuda,Satoshi Shuto.  (2003-03-05)  Control of alpha/beta stereoselectivity in Lewis acid promoted C-glycosidations using a controlling anomeric effect based on the conformational restriction strategy..  Angewandte Chemie (International ed. in English),  42  ((9)): (1021-1023).  [PMID:12616555]
3. Ming Yu,Brian L Pagenkopf.  (2003-11-25)  Allylation of donor--acceptor cyclopropanes..  Organic letters,  ((24)): (4639-4640).  [PMID:14627403]
4. Miriam Romero,Luís Hernández,Leticia Quintero,Fernando Sartillo-Piscil.  (2006-11-08)  Nucleophilic substitution at the anomeric position of 1,2-O-isopropylidenefuranose derivatives. A novel stereoselective synthesis of cyclic phosphates analogous to cAMP..  Carbohydrate research,  341  ((18)): (2883-2890).  [PMID:17087924]
5. Thierry Ollevier,Zhiya Li.  (2007-02-03)  The first catalytic Sakurai reaction of N-alkoxycarbonylamino sulfones with allyltrimethylsilane..  Organic & biomolecular chemistry,  ((24)): (4440-4443).  [PMID:17268636]
6. Shoji Kobayashi,Makiko Hori,Masahiro Hirama.  (2007-12-11)  Synthesis of trans-fused tetrahydrooxepins: stereoselective allylation of sulfur or fluoro-substituted tetrahydrooxepins..  Carbohydrate research,  343  ((3)): (443-452).  [PMID:18068694]
7. Christopher L Rock,Ryan J Trovitch.  (2018-11-30)  Anti-Markovnikov terminal and gem-olefin hydrosilylation using a κ4-diimine nickel catalyst: selectivity for alkene hydrosilylation over ether C-O bond cleavage..  Dalton transactions (Cambridge, England : 2003),  48  ((2)): (461-467).  [PMID:30488914]
8. Roman Schowner,Iris Elser,Mathis Benedikter,Mohasin Momin,Wolfgang Frey,Tanja Schneck,Laura Stöhr,Michael R Buchmeiser.  (2019-11-28)  Origin and Use of Hydroxyl Group Tolerance in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Catalysts..  Angewandte Chemie (International ed. in English),  59  ((2)): (951-958).  [PMID:31774220]

Solution Calculators