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Benzene, 1,3,5-tris(1,1-dimethylethyl)-2-isocyano- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69847-28-5

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69847-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69847-28-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,4 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69847-28:
(7*6)+(6*9)+(5*8)+(4*4)+(3*7)+(2*2)+(1*8)=185
185 % 10 = 5
So 69847-28-5 is a valid CAS Registry Number.

69847-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-tritert-butyl-2-isocyanobenzene

1.2 Other means of identification

Product number -
Other names 2,4,6-tri(tert-butyl)phenyl isonitrile

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:69847-28-5 SDS

69847-28-5Relevant academic research and scientific papers

Reversible intramolecular coupling of the terminal borylene and a carbonyl ligand of [Cp(CO)2Mn=B-tBu]

Braunschweig, Holger,Radacki, Krzysztof,Shang, Rong,Tate, Christopher W.

supporting information, p. 729 - 733 (2013/02/25)

Cyclic complex 2 with bridging carbonyl ligands was synthesized from a facile and reversible intermolecular carbonyl-borylene ligand coupling reaction at room temperature. Complex 2 exhibits an unprecedented coordination mode for boron-metal complexes, which is also reflected in its remarkable 11B NMR chemical shift of -57.2 ppm. Findings from spectroscopic, X-ray, and computational studies are presented, along with a proposed mechanism. Copyright

Fragmentation of an n-substituted one-coordinate phosphorus (Phosphaalkyne): Plausible generation of monovalent phosphorus species

Ionkin, Alex S.,Marshall, William J.,Fish, Brian M.,Howe, Laurie A.

experimental part, p. 4154 - 4158 (2011/01/03)

A new one-step synthesis of a stable nitrogen-substituted phosphaalkyne (5) was developed, by the condensation of CsF (2), tris(trimethylsilyl)phosphine (3), and supermesityl isocyanate (4). Compound 5 has the longest terminal CP bond (1.617 A) of any phosphaalkyne. Due to electron delocalization on the terminal phosphorus atom in 5, fragmentation to a monovalent phosphorus species (CsP (9)) and supermesityl isonitrile (8) is plausible. Isonitrile (8) was isolated in pure form. CsP (9) was trapped as a tricesium pentaphosphorus compound (10) and also as cesium [1,2,4]triphospholide (13).

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