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4-Amino-2-hydroxybenzohydroxamic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35352-91-1

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35352-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35352-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,5 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35352-91:
(7*3)+(6*5)+(5*3)+(4*5)+(3*2)+(2*9)+(1*1)=111
111 % 10 = 1
So 35352-91-1 is a valid CAS Registry Number.

35352-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-N,2-dihydroxybenzamide

1.2 Other means of identification

Product number -
Other names 4-Amino-2-hydroxy-benzohydroxamsaeure

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:35352-91-1 SDS

35352-91-1Upstream product

35352-91-1Downstream Products

35352-91-1Relevant academic research and scientific papers

Three-Dimensional Porous Architectures Based on MnII/III Three-Blade Paddle Wheel Metallacryptates

Marzaroli, Vittoria,Spigolon, Giulia,Lococciolo, Giuseppe,Quaretti, Martina,Salviati, Clarissa,Kampf, Jeff W.,Licini, Giulia,Marchiò, Luciano,Pecoraro, Vincent L.,Tegoni, Matteo

, p. 1954 - 1964 (2019/03/02)

Three metallacryptate supramolecular assemblies have been obtained using salicylhydroxamic acid derivatives (H3L). The three ligands differ in the residue at the para position with respect to the hydroxamic function (-H, -NH2, and -(

Synthesis of hydroxy- and amino-substituted benzohydroxamic acids: Inhibition of ribonucleotide reductase and antitumor activity

van't Riet,Wampler,Elford

, p. 589 - 592 (2007/10/05)

Benzohydroxamic acids inhibit mammalian ribonucleotide reductase and exhibit antineoplastic activity in L1210 leukemic mice. Five new hydroxy- and amino-substituted benzohydroxamic acids (3,4- and 3,5-OH,3,4-NH2, 2,3,4-, and 3,4,5-OH) were prepared and tested along with 12 previously reported benzohydroxamic acids (BHA) for enzyme inhibition and antitumor activity. The most potent enzyme inhibitor in this series was 2,3,4-OH-BHA (ID50=3.5 μM), which is 140 times more potent than hydroxyurea, but its toxicity limited the antitumor activity to a 30% increase in life span of L1210 bearing mice at 125 (mg/kg) day ip for 8 days. The most effective antitumor agent in this series was 3,4-OH-BHA which prolonged the life span of L1210 bearing mice 103% at 600 (mg/kg)/day ip for 8 days.

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