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Acetamide,N,N'-[(tetramethyl-p-phenylene)dimethylene]bis- (6CI,7CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93142-38-2

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93142-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93142-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,1,4 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 93142-38:
(7*9)+(6*3)+(5*1)+(4*4)+(3*2)+(2*3)+(1*8)=122
122 % 10 = 2
So 93142-38-2 is a valid CAS Registry Number.

93142-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[4-(acetamidomethyl)-2,3,5,6-tetramethylphenyl]methyl]acetamide

1.2 Other means of identification

Product number -
Other names 1,2,4,5-Tetramethyl-3,6-bis-acetaminomethyl-benzol

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:93142-38-2 SDS

93142-38-2Downstream Products

93142-38-2Relevant academic research and scientific papers

Supramolecular Paradigm for Capture and Co-Precipitation of Gold(III) Coordination Complexes

Shaffer, Cassandra C.,Liu, Wenqi,Oliver, Allen G.,Smith, Bradley D.

, p. 751 - 757 (2021)

A new supramolecular paradigm is presented for reliable capture and co-precipitation of haloauric acids (HAuX4) from organic solvents or water. Two classes of acyclic organic compounds act as complementary receptors (tectons) by forming two sets of directional non-covalent interactions, (a) hydrogen bonding between amide (or amidinium) NH residues and the electronegative X ligands on the AuX4?, and (b) electrostatic stacking of the electron deficient Au center against the face of an aromatic surface. X-ray diffraction analysis of four co-crystal structures reveals the additional common feature of proton bridged carbonyls as a new and predictable supramolecular design element that creates one-dimensional polymers linked by very short hydrogen bonds (CO???OC distance ?). Two other co-crystal structures show that the amidinium-π???XAu interaction will reliably engage AuX4? with high directionality. These acyclic compounds are very attractive as co-precipitation agents within new “green” gold recovery processes. They also have high potential as tectons for controlled self-assembly or co-crystal engineering of haloaurate composites. More generally, the supramolecular paradigm will facilitate the design of next-generation receptors or tectons with high affinity for precious metal square planar coordination complexes for use in advanced materials, nanotechnology, or medicine.

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