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7178-40-7

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7178-40-7 Usage

Description

4-O-tolylmorpholine, also known as p-Tolylmorpholine, is a chemical compound with the molecular formula C11H15NO. It is a colorless to yellowish liquid with a fruity odor.

Uses

Used in Chemical Industry:
4-O-tolylmorpholine is used as a corrosion inhibitor for its ability to prevent the corrosion of metals, particularly in industrial applications.
Used in Lubricant Industry:
4-O-tolylmorpholine is used as a lubricant additive to enhance the performance and longevity of lubricants in various mechanical systems.
Used in Rubber and Plastics Production:
4-O-tolylmorpholine is used in the production of rubber and plastics due to its ability to improve the properties and performance of these materials.
Used as an Intermediate in Pharmaceutical Synthesis:
4-O-tolylmorpholine is used as an intermediate in the synthesis of pharmaceuticals, contributing to the development of various medications.
Used in Dye Production:
4-O-tolylmorpholine is used in the production of dyes, playing a role in the creation of colorants for various applications.
Used in Agricultural Chemicals:
4-O-tolylmorpholine is used in the synthesis of agricultural chemicals, aiding in the development of products for crop protection and enhancement.
Safety Note:
4-O-tolylmorpholine is considered toxic if ingested, inhaled, or absorbed through the skin, and proper safety measures should be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 7178-40-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7178-40:
(6*7)+(5*1)+(4*7)+(3*8)+(2*4)+(1*0)=107
107 % 10 = 7
So 7178-40-7 is a valid CAS Registry Number.

7178-40-7SDS

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 4-(2-methylphenyl)morpholine

1.2 Other means of identification

Product number -
Other names N-(o-tolyl)morpholine

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:7178-40-7 SDS

7178-40-7Relevant articles and documents

Formal [4+3], [4+2], [4+1] and [2+1] cycloadditions and acid-base reaction of 2-methyl-1,3-dimorpholino-1,3-butadiene with Fischer carbene complexes

Barluenga, Jose,Aznar, Fernando,Fernandez, Monica

, p. 1629 - 1637 (1997)

2-Methyl-1,3-dimorpholino-1,3-butadiene 1 reacted with α,β-unsaturated Fischer carbene complexes to give a wide range of different products depending on the substitution pattern. Thus, seven-membered rings (4, 5 and 6) could be obtained from chromium comp

Synthesis of N-heterocyclic carbene-Pd(II)-5-phenyloxazole complexes and initial studies of their catalytic activity toward the Buchwald-Hartwig amination of aryl chlorides

Zhang, Zhi-Mao,Xu, Yu-Ting,Shao, Li-Xiong

, (2021/04/19)

Three new N-heterocyclic carbene (NHC)-Pd(II) complexes using 5-phenyloxazole as the ancillary ligand have been obtained in moderate to good yields by a one-pot reaction of the corresponding imidazolium salts, palladium chloride and 5-phenyloxazole under mild conditions. Initial studies showed that one of the complexes is an efficient catalyst for the Buchwald-Hartwig amination of aryl chlorides with various secondary and primary amines under the varied catalyst loading of 0.01-0.05 mol%, thus it will enrich the chemistry of NHCs and give an alternative catalyst for the coupling of challenging while cost-low aryl chlorides.

Coupling of Alternating Current to Transition-Metal Catalysis: Examples of Nickel-Catalyzed Cross-Coupling

Bortnikov, Evgeniy O.,Semenov, Sergey N.

supporting information, p. 782 - 793 (2020/12/01)

The coupling of transition-metal to photoredox catalytic cycles through single-electron transfer steps has become a powerful tool in the development of catalytic processes. In this work, we demonstrated that transition-metal catalysis can be coupled to al

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