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(4-MethylMorpholin-3-yl)Methanamine is a chemical substance belonging to the morpholine family, a type of heterocyclic organic compound. It is relatively lesser-known and has limited information available, suggesting that it is not widely used or researched. Morpholines are typically utilized in organic synthesis and serve as intermediates in the production of various pharmaceuticals, agrochemicals, and rubber chemicals. However, the specific applications and properties of (4-MethylMorpholin-3-yl)Methanamine are not well documented.

68431-71-0

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68431-71-0 Usage

Uses

Used in Organic Synthesis:
(4-MethylMorpholin-3-yl)Methanamine is used as a chemical intermediate for the synthesis of various organic compounds. Its presence in the morpholine family suggests that it may be involved in the formation of complex molecules that require heterocyclic structures.
Used in Pharmaceutical Production:
As a member of the morpholine family, (4-MethylMorpholin-3-yl)Methanamine is used as an intermediate in the production of pharmaceuticals. Its role in the synthesis of drug molecules could be crucial for the development of new medications with specific therapeutic properties.
Used in Agrochemical Production:
(4-MethylMorpholin-3-yl)Methanamine is used as a chemical intermediate in the production of agrochemicals. Its potential involvement in the synthesis of compounds with pesticidal or herbicidal properties could contribute to the development of more effective agricultural products.
Used in Rubber Chemical Production:
(4-MethylMorpholin-3-yl)Methanamine is used as an intermediate in the production of rubber chemicals. Its role in the synthesis of compounds that enhance the properties of rubber materials could be significant for the development of improved rubber products with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 68431-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,3 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68431-71:
(7*6)+(6*8)+(5*4)+(4*3)+(3*1)+(2*7)+(1*1)=140
140 % 10 = 0
So 68431-71-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O/c1-8-2-3-9-5-6(8)4-7/h6H,2-5,7H2,1H3

68431-71-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylmorpholin-3-yl)methanamine

1.2 Other means of identification

Product number -
Other names BH2075

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:68431-71-0 SDS

68431-71-0Downstream Products

68431-71-0Relevant academic research and scientific papers

Synthesis and structure-activity relationships of 4-amino-5-chloro-2- ethoxybenzamides with six- and seven-membered heteroalicycles as potential gastroprokinetic agents

Morie,Kato,Harada,Yoshida,Fujiwara,Matsumoto

, p. 1137 - 1147 (2007/10/02)

A new series of 4-amino-5-chloro-2-ethoxybenzamides 3b-f and 5-8 bearing six- and seven-membered heteroalicycles was prepared and evaluated for gastroprokinetic activity. Compounds 3b-e, derived by replacement of the morpholine oxygen of 4-amino-N-[(4-benzyl-2-morpholinyl)methyl]-5-chloro-2- ethoxybenzamide (3a) with other atoms (sulfur, nitrogen and carbon), generally exhibited a potent gastric emptying activity. N-(4-Benzyl-3- morpholinyl)methylbenzamide (5a) and its analogues 5b-e had weaker activity. However, N-(4-benzyl-3-morpholinyl)ethylbenzamide 8 was as potent as 3a. Benzamides 6a-e, having seven-membered heteroalicycles, showed fairly potent activity. Molecular superimpositions of 5a, 6a and 8 upon 3a using computer graphics suggested that the direction of the N-benzyl group greatly influences the gastric emptying activity, whereas the location of the alicyclic nitrogen is less critical.

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