25195-85-1

Basic information

• Product Name: (2-METHYLALLYLOXY)TRIMETHYLSILANE, 95%
• Synonyms: (2-METHYLALLYLOXY)TRIMETHYLSILANE, 95%
• CAS NO: 25195-85-1
• Molecular Formula: C₇H₁₆OSi
• Molecular Weight: 144.28684
• Mol File: 25195-85-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 122°C
• Flash Point: 12°C (54°F)
• Appearance: /
• Refractive Index: 1.4051
• CAS DataBase Reference: (2-METHYLALLYLOXY)TRIMETHYLSILANE, 95%(CAS DataBase Reference)
• NIST Chemistry Reference: (2-METHYLALLYLOXY)TRIMETHYLSILANE, 95%(25195-85-1)
• EPA Substance Registry System: (2-METHYLALLYLOXY)TRIMETHYLSILANE, 95%(25195-85-1)

Safety Data

• Hazardous Substances Data: 25195-85-1(Hazardous Substances Data)

Usage

General Description

(2-Methylallyloxy)trimethylsilane, 95% is a chemical compound with the formula C7H16OSi. It is a colorless liquid with a characteristic odor, and is typically used as an intermediate in the synthesis of various organic compounds. (2-METHYLALLYLOXY)TRIMETHYLSILANE, 95% is commonly employed in the manufacturing of silane coupling agents and as a building block in the production of functionalized silicones. It is also utilized in the preparation of organic molecules for use in a variety of industries, including pharmaceuticals, agrochemicals, and materials science. Additionally, (2-Methylallyloxy)trimethylsilane, 95% has applications in the production of surfactants, adhesives, and coatings. Overall, this chemical is an important reagent for the synthesis of diverse organic compounds and materials.

Upstream product

• 558-30-5 2-methyl-1,2-epoxypropane 
• 27607-77-8 trimethylsilyl trifluoromethanesulfonate 
• 75-77-4 chloro-trimethyl-silane 
• 513-42-8 3-hydroxy-2-methyl-1-propene 
• 66956-92-1 (2-bromo-2-methylpropoxy)trimethylsilane 
• 78-85-3 2-methylpropenal 
• 70582-00-2 1,1,1,3,3-pentamethyldisilazane 
• 18182-35-9 dimethyl(tert-butyl)aminosilane 
• 85696-54-4 cyclopropylmethoxytrimethylsilane 

Downstream Products

• 23483-33-2 2,2,4-Trimethyl-1-oxa-2-sila-cyclopentan 
• 15174-47-7 α-methyl-trans-cinnamaldehyde 
• 86433-25-2 2-<(2-methyl-2-propenyl)oxy>cyclohex-2-enone 
• 139332-46-0 Benzoic acid (2R,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(2-methyl-allyloxy)-tetrahydro-pyran-3-yl ester 

Relevant articles and documents

Total synthesis of formamicin

The enantioselective total synthesis of the cytotoxic plecomacrolide natural product formamicin (1) is described. Key aspects of this synthesis include the efficient transacetalation reactions of MOM ethers 28 and 38 to form the seven-membered formyl acet

Studies on the Total Synthesis of Formamicin: Synthesis of the C(1)-C(11) Fragment

(Matrix Presented) An efficient and highly concise synthesis of 6, corresponding to the C(1)-C(11) fragment of formamicin (1), has been accomplished by a route utilizing a diastereoselective lactate aldol reaction to set the C(6) tertiary ether and the TE

Carbohydrates as chiral auxiliaries: Synthesis of 2-hydroxy-β-D-glucopyranosides

A new 2-step, 1-pot procedure for the stereoselective glycosylation of allylic alcohols with 1,2-di-O-benzoyl-β-D-glucopyranosides to produce 2-hydroxy-β-D-glucopyranosides has been developed. The required precursor for the glycosylation was readily obtained from tri-O-benzyl-D-glucal in 2 steps (91% overall).