Welcome to LookChem.com Sign In|Join Free

CAS

  • or

394-31-0

Post Buying Request

394-31-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

394-31-0 Usage

Chemical Properties

white crystalline powder

Uses

An oral anti-diabetic drug.

Application

5-Hydroxyanthranilic acid can be used as an intermediate of azo and sulfur dyes for the manufacture of photosensitive paper.

Purification Methods

Crystallise the acid from water. The benzamide has m 240-242o (fromAcOH). It is a hypoglycemic agent.[Beilstein 14 H 591, 14 II 357, 14 III 1468, 14 IV 2080.]

Check Digit Verification of cas no

The CAS Registry Mumber 394-31-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 394-31:
(5*3)+(4*9)+(3*4)+(2*3)+(1*1)=70
70 % 10 = 0
So 394-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO3/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3,9H,8H2,(H,10,11)/p-1

394-31-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L08256)  2-Amino-5-hydroxybenzoic acid, 98%   

  • 394-31-0

  • 5g

  • 358.0CNY

  • Detail
  • Alfa Aesar

  • (L08256)  2-Amino-5-hydroxybenzoic acid, 98%   

  • 394-31-0

  • 25g

  • 1458.0CNY

  • Detail
  • Aldrich

  • (278998)  2-Amino-5-hydroxybenzoicacid  98%

  • 394-31-0

  • 278998-5G

  • 477.01CNY

  • Detail

394-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Hydroxyanthranilic acid

1.2 Other means of identification

Product number -
Other names 5-Hydroxyanthranilic

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:394-31-0 SDS

394-31-0Relevant articles and documents

-

Brenans,Prost

, p. 1286 (1924)

-

Catalysis and mechanistic studies of ruthenium and osmium on synthesis of anthranilic acids

Karthikeyan,Jagadeesh, Rajenahally V.,Sree Sandhya,Puttaswamy,Nithya,Kumar, S. Senthil,Bhagat

experimental part, p. 34 - 46 (2011/09/16)

Ruthenium, osmium and ruthenium + osmium catalyzed synthetic methodology was developed for the synthesis of anthranilic acids from indoles in good to excellent yields using bromamine-B in alkaline acetonitrile-water (1:1) at 313 K. Detailed catalysis studies of ruthenium, osmium and the mixture of both were carried out for the synthetic reactions. The positive synergistic catalytic activity of Ru(III) + Os(VIII) was observed to a large extent with the activity greater than the sum of their separate catalytic activities. Detailed kinetic and mechanistic investigations for each catalyzed reactions were carried out. The kinetic pattern and mechanistic picture of each catalyzed reaction were found to be different for each catalyst and to obey the underlying rate laws: rate = k[BAB]t[Indole][Ru(III)]x[OH-] y rate = k[BAB]t[Indole][Os(VIII)][OH-] y rate = k[BAB]t[Indole]o[Ru(III) + Os(VIII)][OH-]y where, x, y Os(VIII) > Ru(III). This trend may be attributed to the different d-electronic configuration of the catalysts. The proposed mechanisms and the rigorous kinetic models derived give results that fit well with the experimental data in each catalyzed reaction. Copyright

Catalytic Cleavage of Active Phosphate and Ester Substrates by Iodoso- and Iodoxybenzoates

Moss, Robert A.,Alwis, K. W.,Shin, Jae-Sup

, p. 2651 - 2655 (2007/10/02)

p-Nitrophenyl acetate, p-nitrophenyl hexanoate, and p-nitrophenyl diphenyl phosphate (PNPDPP) were cleaved by o-iodosobenzoate, o-iodoxybenzoate, and 5-(n-octyloxy)-2-iodosobenzoate (3) in aqueous micellar cetyltrimethylammonium chloride solutions at pH 8.The system 3/CTACl was the best catalyst and PNPDPP was the most reactive substrate.In a remarkably rapid hydrolytic reaction at 25 deg C, 1.0*10-5 M PNPDPP was cleaved by 7.14*10-5 M 3 in 2.0*10-4 M CTACl with kφ=1.04 s-1.Experiments in which > demonstrated that the catalyst "turned over"; i.e., degradation of an intermediate phosphate was not rate limiting.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 394-31-0