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111437-10-6

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111437-10-6 Usage

Description

(5-Amino-2-Methylphenyl)Methanol, also known as 5-Amino-2-methylbenzenemethanol, is an organic compound that serves as a crucial intermediate in the synthesis of various compounds. It is characterized by its amino and methyl groups attached to a phenyl ring, with a hydroxymethyl group as part of its structure. (5-AMino-2-Methylphenyl)Methanol plays a significant role in the production of essential substances, particularly in the pharmaceutical and nutritional industries.

Uses

Used in Pharmaceutical Industry:
(5-Amino-2-Methylphenyl)Methanol is used as an intermediate in the synthesis of 8-Hydroxymethyl Riboflavin, which is an impurity of Riboflavin (R414995). Riboflavin, also known as vitamin B2, is a vital nutritional factor that plays a crucial role in various biological processes. It is found in a wide range of food sources, such as milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source of Riboflavin is yeast, and it is also present in minute amounts in all plant and animal cells. As an enzyme cofactor, Riboflavin is essential for maintaining optimal health and preventing deficiencies.
Used in Nutritional Applications:
(5-Amino-2-Methylphenyl)Methanol is used as a precursor in the production of Riboflavin, which is a vital component of the human diet. Riboflavin is essential for various metabolic processes, including energy production, cellular respiration, and the synthesis of certain amino acids and fatty acids. By contributing to the synthesis of Riboflavin, (5-Amino-2-Methylphenyl)Methanol plays a significant role in ensuring that individuals receive adequate amounts of this essential nutrient, thereby promoting overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 111437-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,3 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 111437-10:
(8*1)+(7*1)+(6*1)+(5*4)+(4*3)+(3*7)+(2*1)+(1*0)=76
76 % 10 = 6
So 111437-10-6 is a valid CAS Registry Number.

111437-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-amino-2-methylphenyl)methanol

1.2 Other means of identification

Product number -
Other names 3-hydroxymethyl-4-methylaniline

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:111437-10-6 SDS

111437-10-6Relevant articles and documents

PYRAZOLE PYRAZINE AMINE COMPOUNDS AS KINASE INHIBITORS, COMPOSITIONS THEREOF AND METHODS OF TREATMENT THEREWITH

-

Page/Page column 128, (2009/09/04)

Provided herein are Pyrazole Pyrazine Amine Compounds having the following structure:Formula (I). Wherein Q and R1-R3 are as defined herein, compositions comprising an effective amount of a Pyrazole Pyrazine Amine Compound and methods for treating or preventing inflammatory conditions, immunological conditions, cancer, neurodegenerative diseases, age-related diseases, cardiovascular diseases and metabolic conditions, or conditions treatable or preventable by inhibition of an IKK, or an IKK pathway, comprising administering an effective amount of a Pyrazole Pyrazine Amine Compound to a patient in need thereof.

One pot preparation of pyrido[2,3,4-de] quinazolines and benzo[de][1,6] naphthyridines by a consecutive process involving an aza-Wittig/ electrocyclic ring-closure/heterocumulene-mediated annelation or intramolecular Diels-Alder cycloaddition sequence

Molina, Pedro,Alajarin, Mateo,Vidal, Angel

, p. 5379 - 5382 (2007/10/02)

Aza Wittig-type reaction of bis(iminophosphorane)1 with one mole of isocyanate leads to the iminophosphoranes 5 which by treatment with a second mole of isocyanate afforded pyrido[2,3,4-de]quinazolines 6. Similarly, reaction with ketenes leads to the formation of benzo[de][1,6] naphthyridines 9. Direct conversion 1→6 and 1→9 were achieved using two moles of isocyanate or ketene respectively.

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