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3439-15-4

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3439-15-4 Usage

Physical state

Colorless, odorless liquid

Uses

Lubricant, personal care products (skin care and hair care), anti-foaming agent, conditioning agent in cosmetics, production of silicone-based materials

Properties

Low surface tension, effective wetting agent, surface tension modifier, thermal stability, resistance to oxidation

Applications

Industrial and consumer applications due to versatile properties

Check Digit Verification of cas no

The CAS Registry Mumber 3439-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3439-15:
(6*3)+(5*4)+(4*3)+(3*9)+(2*1)+(1*5)=84
84 % 10 = 4
So 3439-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H24OSi2/c1-15(2,3)14-16(4,5)12-11-13-9-7-6-8-10-13/h6-10H,11-12H2,1-5H3

3439-15-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-(2-phenylethyl)-trimethylsilyloxysilane

1.2 Other means of identification

Product number -
Other names dimethyl-phenethyl-trimethylsilyloxysilane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3439-15-4 SDS

3439-15-4Downstream Products

3439-15-4Relevant articles and documents

NOVEL ISOCYANIDE COMPOUND, FORMAMIDE COMPOUND, AND METHOD FOR PRODUCING ORGANIC SILICON COMPOUND USING ISOCYANIDE COMPOUND

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Paragraph 0100, (2021/03/19)

To provide a novel isocyanide compound.SOLUTION: The present disclosure provides an isocyanide compound represented by the formula (1). CN-CR1R2-SiR(3-a) (OSiR3R4R5)a (1) [where R1, R2, R3, R4, R5 and R independently represent a hydrogen atom, OR' (R' is a hydrogen atom or an unsubstituted or substituted C1-30 monovalent hydrocarbon group), or an unsubstituted or substituted C1-30 monovalent hydrocarbon group, optionally involving one or more atoms selected from oxygen, nitrogen, sulfur and phosphorus, a is an integer of 1-3].SELECTED DRAWING: Figure 2

Mononuclear iron complex and organic synthesis reaction using same

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Paragraph 25; 26; 27, (2019/08/20)

A mononuclear iron bivalent complex having iron-silicon bonds, which is represented by formula (1), can exhibit an excellent catalytic activity in at least one reaction selected from three reactions, i.e., a hydrosilylation reaction, a hydrogenation reaction and a reaction for reducing a carbonyl compound. (In the formula, R1 to R6 independently represent a hydrogen atom, an alkyl group which may be substituted by X, or the like; X represents a halogen atom, or the like; L1 represents at least one two-electron ligand selected from an isonitrile ligand, an amine ligand, an imine ligand, a nitrogenated heterocyclic ring, a phosphine ligand, a phosphite ligand and a sulfide ligand, wherein, when multiple L1's are present, two L1's may be bonded to each other; L2 represents a two-electron ligand that is different from a CO ligand or the above-mentioned L1, wherein, when multiple L2's are present, two L2's may be bonded to each other; and m1 represents an integer of 1 to 4 and m2 represents an integer of 0 to 3, wherein the sum total of m1 and m2 (i.e., m1+m2) satisfies 3 or 4.)

Cobalt(0) and Iron(0) Isocyanides as Catalysts for Alkene Hydrosilylation with Hydrosiloxanes

Sanagawa, Atsushi,Nagashima, Hideo

supporting information, p. 2859 - 2871 (2018/09/12)

Iron and cobalt isocyanides, Fe(CNR)5 (1) and Co2(CNR)8 (2), where R = t-butyl (tBu), adamantyl (Ad), and mesityl (Mes), were prepared by reduction of FeBr2 or CoI2 in the presence of CNR by C8K or silica-Na. These complexes were subjected to catalytic hydrosilylation of alkenes with hydrosiloxanes, and the results are compared with those obtained by previously reported Fe(OPiv)2/CNAd or Co(OPiv)2/CNAd catalyst systems. Hydrosilylation of allylic ethers with 1,1,1,3,3-pentamethyldisiloxane (PMDS) catalyzed by 1 and the reaction of several alkenes with PMDS or 1,1,1,3,5,5,5-heptamethyltrisiloxane (MD′M) catalyzed by 2 exhibited greater catalytic activity than that observed for the Fe(OPiv)2 or Co(OPiv)2/CNR catalyst system. Complexes 1 and 2 were effective for catalytic chemical modification of silicone fluids containing Si-H groups and for two-component silicone curing. In all cases, selectivity of the reaction in terms of formation of the desired product by hydrosilylation and of byproducts due to dehydrogenative silylation did not differ between the metal isocyanide complexes and the corresponding M(OPiv)2/CNR catalyst system. Catalytically active species generated from 1, 2, and the M(OPiv)2/CNR catalyst system were also investigated.

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