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N-(Hydroxymethyl)salicylamide, also known as salicylanilide, is an organic compound with the molecular formula C8H9NO3. It is a derivative of salicylic acid and contains a hydroxymethyl group. This chemical compound has been studied for its potential pharmaceutical and therapeutic applications, particularly as an anti-inflammatory and analgesic agent. It has also been used as a precursor for the synthesis of other organic compounds. Research on N-(Hydroxymethyl)salicylamide continues to explore its potential uses in medicine and other fields.

13436-87-8

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13436-87-8 Usage

Uses

Used in Pharmaceutical Industry:
N-(Hydroxymethyl)salicylamide is used as an anti-inflammatory and analgesic agent for its potential to alleviate pain and reduce inflammation. Its properties make it a promising candidate for the development of new medications to treat various conditions.
Used in Chemical Synthesis:
N-(Hydroxymethyl)salicylamide is used as a precursor in the synthesis of other organic compounds, contributing to the development of new chemical products and materials. Its versatile structure allows for further modification and functionalization, expanding its applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13436-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,3 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13436-87:
(7*1)+(6*3)+(5*4)+(4*3)+(3*6)+(2*8)+(1*7)=98
98 % 10 = 8
So 13436-87-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3/c10-5-9-8(12)6-3-1-2-4-7(6)11/h1-4,10-11H,5H2,(H,9,12)

13436-87-8SDS

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-hydroxy-N-(hydroxymethyl)benzamide

1.2 Other means of identification

Product number -
Other names Salicylamide,N-(hydroxymethyl)

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:13436-87-8 SDS

13436-87-8Relevant academic research and scientific papers

Synthesis, characterization and biological activity of 1,3,4-substituted 2-azetidinones

Pandey,Gupta,Upadhyay, Mrinalini,Upadhyay, Mridula,Singh,Tandon, Meenal

, p. 158 - 162 (2007/10/03)

Amido/imido alcohol/2-phenyl-3-hydroxyethylquinazolin-4 (3H) -one 1 on treatment with benzoic acid in the presence of cone. H2SO4 yields m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxoquinazolinyl) benzoic acids 2. The acid chloride of 2 on reaction with hydrazine hydrate affords m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxo-quinazolinyl) benzoic acid hydrazides 4 which on condensation with an aromatic aldehyde in acetic acid gives m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxo- quinazolinyl) benzoic acid hydrazones 5. Compounds 5 undergo cyclization with phenoxy acetic acid in the presence of thionyl chloride in dry benzene to furnish 1-[m-(aralkylamido/imidoalkyl/2-phenyl-3-ethyl-3H-4-oxo-quinazolinyl- benzamido)]-3-phenoxy-4-phenyl-2-azetidinones 6. The antiviral and antifungal activities of 6 have been reported.

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