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10219-26-8

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10219-26-8 Usage

General Description

N-Isopropyl-m-toluidine is a chemical compound that is primarily used in the production of rubber and plastic materials. It is an organic compound with the molecular formula C10H15N and a molar mass of 149.23 g/mol. N-ISOPROPYL-M-TOLUIDINE is commonly employed as an intermediate in the manufacturing of antioxidants, rubber accelerators, and dyes. Additionally, N-isopropyl-m-toluidine is utilized in the production of pharmaceuticals and agrochemicals, where it serves as a building block for various active ingredients and intermediates. As a highly versatile chemical, it plays a crucial role in the synthesis of numerous consumer and industrial products, making it an essential component in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 10219-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,1 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10219-26:
(7*1)+(6*0)+(5*2)+(4*1)+(3*9)+(2*2)+(1*6)=58
58 % 10 = 8
So 10219-26-8 is a valid CAS Registry Number.

10219-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-N-propan-2-ylaniline

1.2 Other means of identification

Product number -
Other names 3-Isopropylaminotoluol

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:10219-26-8 SDS

10219-26-8Relevant articles and documents

One-pot reductive amination of acetals with aromatic amines using decaborane (B10H14) in methanol

Park, Eun Soo,Lee, Ji Hee,Kim, Soo Jung,Yoon, Cheol Min

, p. 3387 - 3396 (2003)

Aldehyde acetals and ketone ketals were reductively aminated in one pot with aromatic amines to give the corresponding amines in methanol or aqueous methanol in good to high yields. This direct method might be important because acetals and ketals are used as a popular protecting group for aldehyde and ketones. The advantage of our method is effective even in an aqueous solution and in the application to selective reaction.

Synthesis, reactivities, and catalytic properties of iodo-bridged polymeric iridium complexes with flexible carbon chain-bridged bis(tetramethylcyclopentadienyl) ligands

Tan, Xing,Li, Bin,Xu, Shansheng,Song, Haibin,Wang, Baiquan

, p. 3253 - 3261 (2013/07/19)

Dinuclear iridium complexes [(C5Me4)(CH 2)n(C5Me4)][Ir(COD)]2 (2a: n = 2; 2b: n = 3; 2c: n = 4) are obtained from the reactions of the corresponding dilithium salts Li2/sub

Aminohaloborane in Organic Synthesis. IX. Exclusive ortho Acylation Reaction of N-Monoaminoalkylanilines

Adachi, Makoto,Sasakura, Kazuyuki,Sugasawa, Tsutomu

, p. 1826 - 1835 (2007/10/02)

The exclusive ortho acylation reaction of aniline derivatives using boron trichloride made possible the one-step synthesis of 2-acyl-N-monoaminoalkylanilines (1) and the corresponding imines (2) from N-monoaminoalkylanilines, even in the case of compounds with a bulky substituent at the nitrogen atom.Conventional methods only give 1 via elaborate procedures.Keywords: regioselective reaction; 2-acylaniline derivative; 2-acylaniline-imine derivative; boron trichloride

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