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113003-49-9

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113003-49-9 Usage

General Description

Alpha-Chloro-9-Anthraldoxime is a chemical compound that is most commonly known in scientific research and experiments. Although there is limited information available about this specific substance, like other oximes, it potentially displays reactivity with various chemicals, indicating its possible use in synthetic applications. Oximes are used in many fields, including chemistry, biochemistry, and medicine. However, the toxicity, environmental impact, and potential health effects of Alpha-Chloro-9-Anthraldoxime are not comprehensively documented, suggesting the need for careful handling and further research. It is extremely important to treat this chemical, similar to all chemicals, with the necessary safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 113003-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,0 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113003-49:
(8*1)+(7*1)+(6*3)+(5*0)+(4*0)+(3*3)+(2*4)+(1*9)=59
59 % 10 = 9
So 113003-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H10ClNO/c16-15(17-18)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9,18H/b17-15+

113003-49-9SDS

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 α-CHLORO-9-ANTHRALDOXIME

1.2 Other means of identification

Product number -
Other names A-CHLORO-9-ANTHRALDOXIME

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:113003-49-9 SDS

113003-49-9Downstream Products

113003-49-9Relevant articles and documents

The preparation of intercalating isoxazoles via a nitrile oxide cycloaddition

Mosher,Natale

, p. 779 - 781 (1995)

Pyridinium chlorochromate oxidation of 9-methylacridine (2) affords the corresponding aldehyde 3 in good yield. Conversion of the aldehyde to the hydroximinoyl chloride 5a was accomplished via reaction of the corresponding oxime with N-chlorosuccinimide. Dipolar addition to the enamine of ethylacetoacetate provided the corresponding isoxazoles 1 in good yield.

Highly regioselective 1,3-dipolar cycloaddition of 3′-O-propargyl guanosine with nitrile oxide: An efficient method for the synthesis of guanosine containing isoxazole moiety

Kore, Anilkumar R.,Senthilvelan, Annamalai,Shanmugasundaram, Muthian

, (2020/10/06)

The 1,3-dipolar cycloaddition reaction of 3′-O-propargyl guanosine with various in-situ generated nitrile oxides in the presence of DMF as a solvent is described. It is noteworthy that the reaction is highly regioselective that affords biologically import

(Z)-Stereospecific addition of glycosylmercaptans on nitrilium betaines. Synthesis of 1-S-glucopyranosyl arylthiohydroximates

Brochard,Joseph,Viaud,Rollin

, p. 1403 - 1414 (2007/10/02)

With a view to selecting new internal standards for HPLC analysis of glucosinolates, the synthesis of artificial desulfoglucosinolates 5 was carried out.

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