Welcome to LookChem.com Sign In|Join Free
  • or
CAS:89641-21-4, also known as tetramethylene succinonitrile, is a colorless to pale yellow liquid that serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is a vital building block in the production of substances such as anti-inflammatory drugs and insecticides, and is also utilized in the manufacturing of polymers and as a stabilizer in the electroplating industry. Known for its versatility, tetramethylene succinonitrile has a wide range of applications across different industries.

89641-21-4

Post Buying Request

89641-21-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

89641-21-4 Usage

Uses

Used in Pharmaceutical Industry:
CAS:89641-21-4 is used as an intermediate in the synthesis of various pharmaceuticals for its role in the production of anti-inflammatory drugs and other medicinal compounds.
Used in Agrochemical Industry:
Tetramethylene succinonitrile is used as an intermediate in the synthesis of agrochemicals, specifically for the production of insecticides to protect crops and control pests.
Used in Polymer Industry:
CAS:89641-21-4 is used as a building block in the manufacturing of polymers, contributing to the development of new materials with specific properties for various applications.
Used in Electroplating Industry:
Tetramethylene succinonitrile is used as a stabilizer in the electroplating industry, enhancing the process and improving the quality of the plated surfaces.

Check Digit Verification of cas no

The CAS Registry Mumber 89641-21-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,4 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89641-21:
(7*8)+(6*9)+(5*6)+(4*4)+(3*1)+(2*2)+(1*1)=164
164 % 10 = 4
So 89641-21-4 is a valid CAS Registry Number.

89641-21-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzene-1,3,5-triyltriboronic acid

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:89641-21-4 SDS

89641-21-4Downstream Products

89641-21-4Relevant academic research and scientific papers

A permanent mesoporous organic cage with an exceptionally high surface area

Zhang, Gang,Presly, Oliver,White, Fraser,Oppel, Iris M.,Mastalerz, Michael

, p. 1516 - 1520 (2014)

Recently, porous organic cage crystals have become a real alternative to extended framework materials with high specific surface areas in the desolvated state. Although major progress in this area has been made, the resulting porous compounds are restricted to the microporous regime, owing to the relatively small molecular sizes of the cages, or the collapse of larger structures upon desolvation. Herein, we present the synthesis of a shape-persistent cage compound by the reversible formation of 24 boronic ester units of 12 triptycene tetraol molecules and 8 triboronic acid molecules. The cage compound bears a cavity of a minimum inner diameter of 2.6 nm and a maximum inner diameter of 3.1 nm, as determined by single-crystal X-ray analysis. The porous molecular crystals could be activated for gas sorption by removing enclathrated solvent molecules, resulting in a mesoporous material with a very high specific surface area of 3758 m2 g-1 and a pore diameter of 2.3 nm, as measured by nitrogen gas sorption. Big boronic ester cages: A shape-persistent cuboctahedron can be almost quantitatively formed by a 48-fold one-pot condensation of 12 molecules of a triptycene tetrol with 8 molecules of triboronic acid. The desolvated crystalline material of this cage has a specific surface area of 3758 m2 g-1 and a maximum pore size of 2.3 nm, thus making it mesoporous by the IUPAC definition. Copyright

Self-exfoliation of 2D covalent organic frameworks: Morphology transformation induced by solvent polarity

Zhang, Na,Wang, Taisheng,Wu, Xing,Jiang, Chen,Chen, Fang,Bai, Wei,Bai, Ruke

, p. 3803 - 3808 (2018)

Recently, covalent organic nanosheets (CONs) have emerged as functional two-dimensional (2D) materials for versatile applications. Strong interaction among layers and the instability of borate ester in moisture are the major hurdles to obtain few layered boron-containing CONs by exfoliation of their bulk counterparts. In this paper, we report a facile approach for preparation of few layered borate ester-containing CONs based on electrostatic repulsion of ions. We incorporated organic ionic groups into porous covalent organic frameworks (COFs) and it has been proved that the COFs with quaternary ammonium group could self-exfoliate into few layered ionic covalent organic nanosheets (iCONs) in polar organic solvents. Interestingly, the morphology of the iCOFs-A could be changed from a multilayered aggregation to nanocapsules, or 2D sheets when solvents with different polarity were used. In contrast, non-ionic covalent organic frameworks COFs-B could not self-exfoliate in various solvents. In addition, the self-exfoliated nanosheets could be used to fabricate uniform thin films on SiO2 wafer and the film exhibited explicit optical and electrical properties.

Synthesis of a highly crystalline, covalently linked porous network

-

Page/Page column 3; 13, (2019/05/15)

Porous networks are described linked by boronates. Also described are processes for producing the porous networks. The porous networks are formed by reacting a polyboronic acid with itself or with a polydiol, a polydiamine, or a polyamino alcohol. The res

Inflating face-capped Pd6L8 coordination cages

Jansze, Suzanne M.,Ortiz, Daniel,Fadaei Tirani, Farzaneh,Scopelliti, Rosario,Menin, Laure,Severin, Kay

supporting information, p. 9529 - 9532 (2018/08/28)

Tritopic metalloligands were used to form two Pd6L8-type coordination cages. With molecular weights of more than 15 kDa and Pd?Pd distances of up to 4.2 nm, these complexes are among the largest palladium cages described to date.

A Photoresponsive Smart Covalent Organic Framework

Huang, Ning,Ding, Xuesong,Kim, Jangbae,Ihee, Hyotcherl,Jiang, Donglin

, p. 8704 - 8707 (2015/11/27)

Ordered π-columnar structures found in covalent organic frameworks (COFs) render them attractive as smart materials. However, external-stimuli-responsive COFs have not been explored. Here we report the design and synthesis of a photoresponsive COF with anthracene units as the photoresponsive π-building blocks. The COF is switchable upon photoirradiation to yield a concavo-convex polygon skeleton through the interlayer [4π+4π] cycloaddition of anthracene units stacked in the π-columns. This cycloaddition reaction is thermally reversible; heating resets the anthracene layers and regenerates the COF. These external-stimuli-induced structural transformations are accompanied by profound changes in properties, including gas adsorption, π-electronic function, and luminescence. The results suggest that COFs are useful for designing smart porous materials with properties that are controllable by external stimuli.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 89641-21-4