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71835-14-8

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71835-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71835-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,3 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71835-14:
(7*7)+(6*1)+(5*8)+(4*3)+(3*5)+(2*1)+(1*4)=128
128 % 10 = 8
So 71835-14-8 is a valid CAS Registry Number.

71835-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-carboxyanilino)-4-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Nitro-2,2'-imino-di-benzoesaeure

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:71835-14-8 SDS

71835-14-8Relevant articles and documents

Use of N,N-dimethylformamide as solvent in the synthesis of N-phenylanthranilic acids

Pellon, Rolando F.,Carrasco, Ramon,Marquez, Tania,Mamposo, Taimirys

, p. 5107 - 5110 (1997)

It is known that N-phenylanthranilic acids can be synthesized by Ullmann-Goldberg condensation in different conditions. This paper reports some parameters which influence the condensation and reports a general procedure for this reaction using N,N-Dimethylformamide as solvent.

Fast synthesis of substituted N-phenylanthranilic acids using Ullmann condensation under microwave irradiation in dry media

Martin, Ana,Mesa, Miriam,Docampo, Maite L.,Gomez, Victoria,Pellon, Rolando F.

, p. 271 - 277 (2007/10/03)

Substituted N-phenylanthranilic acids using the Ullmann condensation under microwave irradiation in dry media were obtained in good yield and short reaction times. Copyright Taylor & Francis LLC.

Synthesis of Substituted 9-Oxo-9,10-dihydroacridine-4-carboxylic Acids. I. Factors Affecting the Direction of Ring Closure of Substituted N-(2-Carboxyphenylamino)benzoic Acids

Stewart, Georgina M.,Rewcastle, Gordon W.,Denny, William A.

, p. 1939 - 1950 (2007/10/02)

The cyclodehydration of 16 substituted N-(2-carboxyphenylamino)benzoic acids to substituted 9-oxo-9,10-dihydroacridine-4-carboxylic acids with conc.H2SO4, POCl3 and ethyl polyphosphate (epp) has been studied by h.p.l.c.Direction of ring closure can be qua

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