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N,N-Diisopropyl-3-methoxyaniline, an aniline derivative with the molecular formula C13H21NO, features two isopropyl groups and a methoxy group attached to the nitrogen atom. This colorless to pale yellow liquid with a characteristic odor is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as a catalyst in various organic reactions. Due to its potential to cause irritation to the skin, eyes, and respiratory system, it should be handled with care.

7000-87-5

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7000-87-5 Usage

Uses

Used in Pharmaceutical Industry:
N,N-Diisopropyl-3-methoxyaniline is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving the efficacy of existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, N,N-Diisopropyl-3-methoxyaniline serves as an intermediate in the production of agrochemicals, aiding in the creation of more effective pesticides and other agricultural chemicals.
Used as a Catalyst in Organic Reactions:
N,N-Diisopropyl-3-methoxyaniline is utilized as a catalyst in a range of organic reactions, enhancing the efficiency and selectivity of these processes, which is crucial for the synthesis of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 7000-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7000-87:
(6*7)+(5*0)+(4*0)+(3*0)+(2*8)+(1*7)=65
65 % 10 = 5
So 7000-87-5 is a valid CAS Registry Number.

7000-87-5SDS

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 N,N-Diisopropyl-3-methoxyaniline

1.2 Other means of identification

Product number -
Other names 3-methoxy-N,N-di(propan-2-yl)aniline

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:7000-87-5 SDS

7000-87-5Downstream Products

7000-87-5Relevant academic research and scientific papers

The anionic thia-Fries rearrangement of aryl triflates

Charmant, Jonathan P. H.,Dyke, Alan M.,Lloyd-Jones, Guy C.

, p. 380 - 381 (2007/10/03)

Aryl triflates undergo LDA-mediated rearrangement to generate o-hydroxyaryl trifluoromethylsulfones. In some cases, partitioning between rearrangement and aryne generation can be controlled.

Benzyne Generation from Aryl Triflates

Wickham, Peter P.,Hazen, Kevin H.,Guo, Hong,Jones, Garth,Reuter, Kelly Hardee,Scott, William J.

, p. 2045 - 2050 (2007/10/02)

The use of aryl triflates to form arynes as reactive intermediates is decribed.This allows the first general use of phenols as aryne precursors.Phenyl triflate reacts with LDA at -78 deg C to form benzyne, which then reacts with diisopropylamine generating N,N-diisopropylaniline.Yields of diisopropylarylamines from aryne intermediates are superior to those previously reported.Regioisomeric ratios are similar to those obtained with use of other benzyne precursors.

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