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(2,4,6-trimethylbenzyl)propanedinitrile is a chemical compound with the molecular formula C13H15N. It is a dinitrile derivative of 2,4,6-trimethylbenzylpropane, characterized by its unique chemical structure and properties.
Used in Fragrance Industry:
(2,4,6-trimethylbenzyl)propanedinitrile is used as a fragrance ingredient for its fruity, floral, and slightly sweet aroma. It is popular in the production of perfumes and personal care products, adding pleasant scents to various consumer goods.
Used in Organic Synthesis and Materials Science:
(2,4,6-trimethylbenzyl)propanedinitrile may also have potential applications in the field of organic synthesis and materials science due to its unique chemical structure and properties. However, it is important to handle this chemical with care and adhere to proper safety protocols when working with it.

5553-88-8

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5553-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5553-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5553-88:
(6*5)+(5*5)+(4*5)+(3*3)+(2*8)+(1*8)=108
108 % 10 = 8
So 5553-88-8 is a valid CAS Registry Number.

5553-88-8SDS

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 2-[(2,4,6-trimethylphenyl)methyl]propanedinitrile

1.2 Other means of identification

Product number -
Other names -

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:5553-88-8 SDS

5553-88-8Relevant academic research and scientific papers

Preparation of O-Protected Cyanohydrins by Aerobic Oxidation of α-Substituted Malononitriles in the Presence of Diarylphosphine Oxides

Zhang, Dapeng,Lian, Mingming,Liu, Jia,Tang, Shukun,Liu, Guangzhi,Ma, Cunfei,Meng, Qingwei,Peng, Haisheng,Zhu, Daling

supporting information, p. 2597 - 2601 (2019/04/17)

A mild, reagent-cyanide-free, and efficient synthesis of O-phosphinoyl-protected cyanohydrins from readily available α-substituted malononitriles was realized using diarylphosphine oxides in the presence of O2. Mechanistic studies indicated that in addition to the initial aerobic oxidation of the malononitrile derivative notable features of this process include the formation of a tetrahedral intermediate and a subsequent intramolecular rearrangement. The phosphinoyl-protecting group can be removed by alcoholysis or by reduction with DIBAL-H.

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