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p-aminophenyl isocyanide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69236-29-9

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69236-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69236-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,3 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69236-29:
(7*6)+(6*9)+(5*2)+(4*3)+(3*6)+(2*2)+(1*9)=149
149 % 10 = 9
So 69236-29-9 is a valid CAS Registry Number.

69236-29-9SDS

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 p-aminophenyl isocyanide

1.2 Other means of identification

Product number -
Other names 4-isocyanophenylamine

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:69236-29-9 SDS

69236-29-9Downstream Products

69236-29-9Relevant academic research and scientific papers

Method for preparing isonitrile compound

-

Paragraph 0044-0049, (2021/01/30)

The invention discloses a method for preparing an isonitrile compound, and belongs to the field of organic synthesis. According to the method, sodium chlorodifluoroacetate or potassium bromodifluoroacetate is used as a difluoromethyl source and is condensed with primary amine under the action of alkali to obtain an isocyanide target product, so that isocyanide is generated in situ on the primary amine. The reaction raw materials, alkali and solvent used in the method are simple and easy to obtain, wide in source and convenient to operate, do not need special storage and use conditions, the method has the advantages of safety, low cost, high yield, simple process, environmental friendliness and the like, and has important application value in the fields of medicine, protein and polypeptidepreparation, pesticides, high polymer materials, dyes and the like.

Synthesis of isocyanides by reacting primary amines with difluorocarbene

Si, Yi-Xin,Zhu, Peng-Fei,Zhang, Song-Lin

supporting information, p. 9086 - 9090 (2020/11/30)

A general, convenient, and friendly route for preparing a versatile building block of isocyanides from primary amines is developed. Difluorocarbene, generated in situ from decarboxylation of chlorodifluoroacetate, reacts efficiently with primary amines to produce isocyanides. Various primary amines are well tolerated, including aryl, heteroaryl, benzyl, and alkyl amines, as well as amine residues in amino acids and peptides. Late-stage functionalization of biologically active amines is demonstrated, showing its practical capacity in drug design and peptide modification.

Stepwise Assembly of Mixed Metal Dinuclear Carbonyl Complexes

Heinze, Katja,Jacob, Volker

, p. 3918 - 3923 (2007/10/03)

The one-pot/three-step solution synthesis of a library of nine directional, dinuclear mixed-metal complexes composed of different metal-carbonyl units (M = Cr, Mo, W) and a bifunctional bridging isocyanide Schiff-base ligand is described. The well-defined

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