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104333-09-7

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104333-09-7 Usage

General Description

4-AMINO-2-(HYDROXYMETHYL)BENZENOL is a chemical compound with the molecular formula C7H9NO2. It is also known as 4-aminosyrenol and has a molecular weight of 139.15 g/mol. 4-AMINO-2-(HYDROXYMETHYL)BENZENOL is a member of the aminophenol class of chemicals and contains both amino and hydroxymethyl functional groups, making it useful in various chemical reactions and processes. It is used in the production of pharmaceuticals, dyes, and as a precursor in organic synthesis. Additionally, it has antimicrobial and antioxidant properties, making it potentially useful in medical and cosmetic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 104333-09-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,3,3 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104333-09:
(8*1)+(7*0)+(6*4)+(5*3)+(4*3)+(3*3)+(2*0)+(1*9)=77
77 % 10 = 7
So 104333-09-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2/c8-6-1-2-7(10)5(3-6)4-9/h1-3,9-10H,4,8H2

104333-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-2-(hydroxymethyl)phenol

1.2 Other means of identification

Product number -
Other names 2-hydroxymethyl-para-aminophenol

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:104333-09-7 SDS

104333-09-7Relevant articles and documents

MODULATION OF IMMUNE CELLS

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Paragraph 0049; 00126-00127, (2021/08/06)

Disclosed are immune cell-selective small molecule IMPDH inhibitor compounds and methods of their synthesis and use to treat proliferative disorders.

Synthesis of a bis-azido analogue of acromelic acid for radioisotope-free photoaffinity labeling and biochemical studies

Sun, Pi,Wang, Guang Xing,Furuta, Kyoji,Suzuki, Masaaki

, p. 2433 - 2436 (2007/10/03)

A novel acromelic acid analogue containing a phenyl group possessing two different types of azido functional groups, of which one is the aromatic N 3 acting as a photoaffinity group to bind to a target protein by photoirradiation and the other

One step hair coloring compositions using salts

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, (2008/06/13)

A hair coloring composition comprising the following two compositions which are mixed just prior to application to the hair: (a) a composition comprising a water-soluble peroxygen oxidizing agent; and (b) a composition comprising one or more oxidative hair coloring agents selected from the group consisting of an aromatic diamine, an amino phenol, a naphthol, a polyhydric phenol, a catechol and mixtures thereof; wherein the composition comprising one or more oxidative hair coloring agents further comprises al least one water soluble carbonate releasing salts; and optionally a water soluble ammonium salt, is described.

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