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70261-50-6

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70261-50-6 Usage

Description

2,6-diMethyl-3-(phenylMethoxy)-benzenaMine is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals and chemicals. It is characterized by its unique molecular structure, which includes two methyl groups and a phenylmethoxy group attached to a benzene ring.

Uses

Used in Pharmaceutical Industry:
2,6-diMethyl-3-(phenylMethoxy)-benzenaMine is used as a key intermediate in the synthesis of Mepivacaine (M225060) metabolites. Mepivacaine is a widely used local anesthetic drug, and the synthesis of its metabolites is essential for understanding its pharmacokinetics, efficacy, and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 70261-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,2,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70261-50:
(7*7)+(6*0)+(5*2)+(4*6)+(3*1)+(2*5)+(1*0)=96
96 % 10 = 6
So 70261-50-6 is a valid CAS Registry Number.

70261-50-6SDS

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 3-amino-2,4-dimethylphenyl benzyl ether

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-3-(phenylmethoxy)-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:70261-50-6 SDS

70261-50-6Relevant articles and documents

Amidinoureas substituted in both the urea and amidino nitrogen positions

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, (2008/06/13)

A method of inducing blood pressure reduction in humans and mammals by administering 2,6-disubstituted phenyl N-alkyl amidinoureas in which the phenyl ring is additionally substituted by a hydroxy, alkoxy, aralkoxy, alkenyloxy, alkynyloxy, acyloxy or halo acyloxy group and a novel class of amidinourea compounds having pharmaceutical uses, including blood pressure lowering activity.

BLOOD PRESSURE LOWERING AND ADRENERGIC BETA -RECEPTOR INHIBITING 3-(4-PHENOXYMETHYLPIPERIDINO)-PROPYL-PHENYL ETHERS

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, (2008/06/13)

A 3-(4-phenoxymethylpiperidino)-propyl-phenyl-ether of the formula STR1 wherein R 1 and R 2 each independently is hydrogen, lower alkyl, hydroxyalkyl, lower alkanoyloxyalkyl or--CO--Z, Z is hydroxy, lower alkyloxy or STR2 R 6 and R. sub.7 each inde

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