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BIPHENYLDIISOPROPYLSILYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136449-55-3

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136449-55-3 Usage

Chemical Properties

white low melting solid

Check Digit Verification of cas no

The CAS Registry Mumber 136449-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,4 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136449-55:
(8*1)+(7*3)+(6*6)+(5*4)+(4*4)+(3*9)+(2*5)+(1*5)=143
143 % 10 = 3
So 136449-55-3 is a valid CAS Registry Number.

136449-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name BIPHENYLDIISOPROPYLSILYL CHLORIDE

1.2 Other means of identification

Product number -
Other names P-BIPHENYL-DIISOPROPYLSILYL CHLORIDE

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:136449-55-3 SDS

136449-55-3Downstream Products

136449-55-3Relevant academic research and scientific papers

Crown Ether Nucleophilic Catalysts (CENCs): Agents for Enhanced Silicon Radiofluorination

Jana, Susovan,Al-Huniti, Mohammed H.,Yang, Bo Yeun,Lu, Shuiyu,Pike, Victor W.,Lepore, Salvatore D.

, p. 2329 - 2335 (2017/03/11)

New bifunctional phase transfer agents were synthesized and investigated for their abilities to promote rapid fluorination at silicon. These agents, dubbed crown ether nucleophilic catalysts (CENCs), are 18-crown-6 derivatives containing a side-arm and a potentially nucleophilic hydroxyl group. These CENCs proved efficacious in the fluorination of hindered silicon substrates, with fluorination yields dependent on the length of linker connecting the metal chelating unit to the hydroxyl group. The efficacy of these CENCs was also demonstrated for rapid radiofluorination under mild conditions for eventual application in molecular imaging with positron emission tomography (PET). The hydrolysis-resistant aryl silicon fragment is promising as a convenient synthon for labeling potential PET radiotracers.

Amino acid-promoted C-H alkylation with alkylboronic acids using a removable directing group

Zhang, Yanghui,Zhang, Yu,Jiang, Hang,Chen, Dushen

supporting information, p. 4585 - 4589 (2016/06/09)

Palladium-catalyzed C-H alkylation reaction with alkylboronic acids has successfully been developed using a removable pyridyldiisopropylsilyl directing group. The amino acid played a crucial role as a ligand in the reaction. The alkylation protocol is also applicable to the coupling of C(sp3)-H bonds with alkylboronic acids.

Biphenyldialkylsilyl chlorides: Reagents for the formation of crystalline derivatives of small terminal alkynes

Anthony,Diederich

, p. 3787 - 3790 (2007/10/02)

Biphenyldimethylsilyl chloride (BDMS-Cl) and biphenyldiisopropylsilyl chloride (BDIPS-Cl) are readily prepared reagents for the introduction of the BDMS and BDIPS protecting groups onto small terminal alkynes, leading to stable, solid, and easily recrystallizable derivatives of these thermally unstable molecules.

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