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Silane, dichloro(chloromethyl)(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90003-84-2

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90003-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90003-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,0 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90003-84:
(7*9)+(6*0)+(5*0)+(4*0)+(3*3)+(2*8)+(1*4)=92
92 % 10 = 2
So 90003-84-2 is a valid CAS Registry Number.

90003-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl-dichloro-(chloromethyl)silane

1.2 Other means of identification

Product number -
Other names benzyl-dichloro-chloromethyl-silane

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:90003-84-2 SDS

90003-84-2Relevant academic research and scientific papers

Pentacoordinate hydrochlorosilanes with lactamomethyl ligand

Pestunovich, Vadim A.,Kirpichenko, Svetlana V.,Lazareva, Natal'ya F.,Albanov, Aleksander I.,Voronkov, Mikhail G.

, p. 2160 - 2167 (2007)

The synthesis and reaction behavior of pentacoordinate hydrochlorosilanes LCH2SiRHCl (L- 2-piperidonyl ligand, R = Me, Ph, Bn) are described. The intramolecular O-Si and N-Si coordination is discussed on the basis of the NMR data. The strength

Kinetic Resolution of Tertiary Propargylic Alcohols by Enantioselective Cu?H-Catalyzed Si?O Coupling

Seliger, Jan,Dong, Xichang,Oestreich, Martin

supporting information, p. 1970 - 1974 (2019/01/29)

A broad range of tertiary propargylic alcohols were kinetically resolved by catalyst-controlled enantioselective silylation. This non-enzymatic kinetic resolution is catalyzed by a Cu?H species and makes use of the commercially available precatalyst MesCu/(R,R)-Ph-BPE and a simple hydrosilane as the resolving reagent. Both alkyl,aryl- as well as dialkyl-substituted propargylic alcohols participate, and especially high selectivity factors are achieved when the alkyne terminus carries a TIPS group, which also enables facile post-functionalization in this position (s up to 207).

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