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5-Methoxyanthranilic acid HCL is a chemical compound derived from anthranilic acid, which is a common building block in the synthesis of various pharmaceuticals and dyes. It is a yellow crystalline powder that is slightly soluble in water and ethanol.

1882-70-8

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1882-70-8 Usage

Uses

Used in Pharmaceutical Industry:
5-Methoxyanthranilic acid HCL is used as a key intermediate in the synthesis of several anti-inflammatory and anti-microbial drugs. Its unique chemical structure allows for the development of effective medications to combat inflammation and infections.
Used in Dye and Pigment Industry:
5-Methoxyanthranilic acid HCL is used in the production of dyes and pigments, providing vibrant colors and enhancing the stability of these products. Its chemical properties contribute to the creation of high-quality dyes for various applications.
Used in Fluorescent Dye Manufacturing:
5-Methoxyanthranilic acid HCL is employed in the manufacturing of fluorescent dyes, which are essential for various scientific and industrial applications, including microscopy, diagnostics, and imaging techniques.
Used in Ultraviolet Light Absorber Production:
5-Methoxyanthranilic acid HCL is used in the production of ultraviolet light absorbers, which are crucial for protecting materials and surfaces from the damaging effects of UV radiation. Its presence in these products helps to extend their lifespan and maintain their integrity.
Used in Organic Compound Synthesis for Research and Industrial Applications:
5-Methoxyanthranilic acid HCL serves as a building block in the synthesis of various organic compounds for research and industrial applications. Its versatile chemical properties make it a valuable component in the development of new compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 1882-70-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1882-70:
(6*1)+(5*8)+(4*8)+(3*2)+(2*7)+(1*0)=98
98 % 10 = 8
So 1882-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3.ClH/c1-12-5-2-3-7(9)6(4-5)8(10)11;/h2-4H,9H2,1H3,(H,10,11);1H

1882-70-8SDS

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-amino-5-methoxybenzoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 5-Methoxyanthranilic acid hydrochloride

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:1882-70-8 SDS

1882-70-8Relevant academic research and scientific papers

Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids Dedicated to Professor Slovenko Polanc on his 65th birthday

Kafka, Stanislav,Proisl, Karel,Ka?párková, Věra,Urankar, Damijana,Kimmel, Roman,Ko?mrlj, Janez

, p. 10826 - 10835 (2014/01/06)

N-(α-Ketoacyl)anthranilic acids were prepared by oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones by using paraperiodic acid (H5IO6) or sodium periodate (NaIO4). The optimisation of the reaction conditions is

SYNTHETIC ANALOGS OF Peganum ALKALOIDS. I. SYNTHESIS OF METHOXY- AND HYDROXY-SUBSTITUTED DEOXYVASICINONES AND DEOXYPEGANINES

Karimov, A.,Telezhenetskaya, M. V.,Yunusov, S. Yu.

, p. 466 - 472 (2007/10/02)

6-Methoxy-, 7-methoxy-, and 8-methoxydeoxyvasicinones have been synthesized by the reaction of substituted (3-methoxy-, 4-methoxy-, and 5-methoxy-) anthranilic acids with α-pyrrolidone.The demethylation of these compounds has given the corresponding hydroxy-substituted analogs of deoxyvasicinone, and the reduction of the products obtained with zinc in hydrochloric acid has given the hydroxy- and methoxy- analogs of deoxypeganine. 8-Hydrooxydeoxypeganine dimethyl-, ethyl-, and butylcarbamates have been obtained by the carbamoylation of 8-hydroxydeoxypeganine.

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