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107411-34-7

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107411-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107411-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,1 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107411-34:
(8*1)+(7*0)+(6*7)+(5*4)+(4*1)+(3*1)+(2*3)+(1*4)=87
87 % 10 = 7
So 107411-34-7 is a valid CAS Registry Number.

107411-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-N,N-dipropyl aniline

1.2 Other means of identification

Product number -
Other names N,N-Dipropyl-o-anisidine

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:107411-34-7 SDS

107411-34-7Relevant articles and documents

A 3 - (dipropyl amino) -4 - methoxybenzene sulfonic acid

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Paragraph 0029-0031, (2017/05/26)

The invention belongs to the field of chemical synthesis, and discloses a method for preparing 3-(dipropyl amino)-4-methoxyl benzenesulfonic acid. The 3-(dipropyl amino)-4-methoxyl benzenesulfonic acid takes 2-anisidine as the raw material and is prepared through two steps of reaction. The invention provides the synthesis method for the 3-(dipropyl amino)-4-methoxyl benzenesulfonic acid for the first time, and offers the synthesis route for preparation of the 3-(dipropyl amino)-4-methoxyl benzenesulfonic acid; and the preparation method is simple, has high yield and low cost, and can be used for large-scale production.

Indolyl phthalide compounds

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, (2008/06/13)

3-Aryl-3-indolylphthalides, 3-aryl-3-pyrrolylphthalides and 3-aryl-3-carbazolylphthalides prepared by interaction of the appropriate 2-(heteroaryl)carbonylbenzoic acid and the appropriate phenylamine, and 3,3-bis(indolyl)phthalides prepared by the interaction of the appropriate 2-(indolyl)carbonylbenzoic acid and the appropriate indole are useful as color formers in pressure-sensitive carbonless duplicating systems, thermal marking systems and hectographic copying systems.

Phthalide compounds, processes and marking systems

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, (2008/06/13)

3-Aryl-3-indolylphthalides, 3-aryl-3-pyrrolylphthalides and 3-aryl-3-carbazolylphthalides prepared by interaction of the appropriate 2-(heteroaryl)carbonylbenzoic acid and the appropriate phenylamine, and 3,3-bis(indolyl)phthalides prepared by the interaction of the appropriate 2-(indolyl)carbonylbenzoic acid and the appropriate indole are useful as color formers in pressure-sensitive carbonless duplicating systems, thermal marking systems and hectographic copying systems.

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