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7000-87-5

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7000-87-5 Usage

General Description

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

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 articles and documents

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.

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