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25374-10-1

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25374-10-1 Usage

General Description

BIS(DIMETHYLAMINO)PHENYLCHLOROSILANE is a chemical compound with the molecular formula C10H17ClN2Si. It is a chlorosilane with two dimethylamino groups and a phenyl group attached to a silicon atom. BIS(DIMETHYLAMINO)PHENYLCHLOROSILANE is commonly used as a reagent in organic synthesis, particularly in the formation of silicon-containing polymers and materials. BIS(DIMETHYLAMINO)PHENYLCHLOROSILANE is also used as a coupling agent in the preparation of functionalized silanes for surface modification and as a precursor for silicon-based materials in electronic applications. It is important to handle this chemical with care, as it is highly reactive with water and can produce toxic fumes when heated.

Check Digit Verification of cas no

The CAS Registry Mumber 25374-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,3,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25374-10:
(7*2)+(6*5)+(5*3)+(4*7)+(3*4)+(2*1)+(1*0)=101
101 % 10 = 1
So 25374-10-1 is a valid CAS Registry Number.

25374-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[chloro-(dimethylamino)-phenylsilyl]-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names EINECS 246-907-7

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:25374-10-1 SDS

25374-10-1Downstream Products

25374-10-1Relevant articles and documents

Chloraminosilanes II. Preparation and spectroscopic studies on alkyl-(dimethylamino)chlorosilanes

Washburne,Peterson Jr.

, p. 59 - 64 (2007/10/12)

Several new compounds containing both chloro and dimethylamino groups linked to silicon have been prepared. The general method involved reacting a solution of the appropriate polychlorosilane in ether at ca. - 50° with a chilled ethereal solution of dimethylamine. Prepared in this fashion were CH3Si(NMe2)Cl2, CH3Si(NMe2)2-Cl, PhSi(NMe2)Cl2, PhSi(NMe2)2Cl, CH3(H)Si(NMe2)Cl, (CH3)2Si(NMe2)Cl, CH2CH(CH3)Si(NMe2)Cl, and Ph2Si(NMe2)Cl. Comparison of the spectra of these compounds with those in the perhalo and peramine series showed that replacement of NMe2 for Cl resulted in an upfield shift of the resonances of the other groups linked to silicon, a shift which parallels that observed upon substitution of CH3 for Cl. The relationship of ν(SiH) in the IR and δ(SiH) in the NMR spectra was linear.

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